List of Excipients in API moxifloxacin hydrochloride
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Excipients in NDA-approved (novel) drugs containing moxifloxacin hydrochloride
Company | Tradename | Ingredient | NDC | Excipient | Potential Generic Entry |
---|---|---|---|---|---|
Alcon Laboratories Inc | MOXEZA | moxifloxacin hydrochloride | 0065-0006 | BORIC ACID | |
Alcon Laboratories Inc | MOXEZA | moxifloxacin hydrochloride | 0065-0006 | HYDROCHLORIC ACID | |
Alcon Laboratories Inc | MOXEZA | moxifloxacin hydrochloride | 0065-0006 | SODIUM CHLORIDE | |
Alcon Laboratories Inc | MOXEZA | moxifloxacin hydrochloride | 0065-0006 | SODIUM HYDROXIDE | |
>Company | >Tradename | >Ingredient | >NDC | >Excipient | >Potential Generic Entry |
Excipients in ANDA-approved (generic) drugs containing moxifloxacin hydrochloride
Company | Ingredient | NDC | Excipient |
---|---|---|---|
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 | CELLULOSE, MICROCRYSTALLINE |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 | CROSCARMELLOSE SODIUM |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 | FERRIC OXIDE RED |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 | HYPROMELLOSE 2910 |
>Company | >Ingredient | >NDC | >Excipient |
Detailed excipient profiles for moxifloxacin hydrochloride
Excipient focus: ANHYDROUS LACTOSE
moxifloxacin hydrochloride drug variants containing ANHYDROUS LACTOSE
moxifloxacin hydrochloride drug variants not containing ANHYDROUS LACTOSE
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
>Company | >Ingredient | >NDC |
Excipient focus: BORIC ACID
moxifloxacin hydrochloride drug variants containing BORIC ACID
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
Upsher-Smith Laboratories LLC | moxifloxacin hydrochloride | 0832-1410 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing BORIC ACID
Excipient focus: CELLULOSE, MICROCRYSTALLINE
moxifloxacin hydrochloride drug variants containing CELLULOSE, MICROCRYSTALLINE
moxifloxacin hydrochloride drug variants not containing CELLULOSE, MICROCRYSTALLINE
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
Upsher-Smith Laboratories LLC | moxifloxacin hydrochloride | 0832-1410 |
>Company | >Ingredient | >NDC |
Excipient focus: COPOVIDONE K25-31
moxifloxacin hydrochloride drug variants containing COPOVIDONE K25-31
moxifloxacin hydrochloride drug variants not containing COPOVIDONE K25-31
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
>Company | >Ingredient | >NDC |
Excipient focus: CROSCARMELLOSE SODIUM
moxifloxacin hydrochloride drug variants containing CROSCARMELLOSE SODIUM
moxifloxacin hydrochloride drug variants not containing CROSCARMELLOSE SODIUM
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
Upsher-Smith Laboratories LLC | moxifloxacin hydrochloride | 0832-1410 |
>Company | >Ingredient | >NDC |
Excipient focus: FERRIC OXIDE RED
moxifloxacin hydrochloride drug variants containing FERRIC OXIDE RED
moxifloxacin hydrochloride drug variants not containing FERRIC OXIDE RED
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
Upsher-Smith Laboratories LLC | moxifloxacin hydrochloride | 0832-1410 |
>Company | >Ingredient | >NDC |
Excipient focus: FERROSOFERRIC OXIDE
moxifloxacin hydrochloride drug variants containing FERROSOFERRIC OXIDE
Company | Ingredient | NDC |
---|---|---|
Novel Laboratories Inc | moxifloxacin hydrochloride | 40032-034 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing FERROSOFERRIC OXIDE
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
>Company | >Ingredient | >NDC |
Excipient focus: HYDROCHLORIC ACID
moxifloxacin hydrochloride drug variants containing HYDROCHLORIC ACID
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
Upsher-Smith Laboratories LLC | moxifloxacin hydrochloride | 0832-1410 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing HYDROCHLORIC ACID
Excipient focus: HYPROMELLOSE 2910
moxifloxacin hydrochloride drug variants containing HYPROMELLOSE 2910
moxifloxacin hydrochloride drug variants not containing HYPROMELLOSE 2910
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
Upsher-Smith Laboratories LLC | moxifloxacin hydrochloride | 0832-1410 |
>Company | >Ingredient | >NDC |
Excipient focus: HYPROMELLOSES
moxifloxacin hydrochloride drug variants containing HYPROMELLOSES
Company | Ingredient | NDC |
---|---|---|
Novel Laboratories Inc | moxifloxacin hydrochloride | 40032-034 |
Sunshine Lake Pharma Co Ltd | moxifloxacin hydrochloride | 48792-7823 |
Physicians Total Care Inc | moxifloxacin hydrochloride | 54868-4367 |
RedPharm Drug Inc | moxifloxacin hydrochloride | 67296-0154 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing HYPROMELLOSES
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
>Company | >Ingredient | >NDC |
Excipient focus: LACTOSE MONOHYDRATE
moxifloxacin hydrochloride drug variants containing LACTOSE MONOHYDRATE
Company | Ingredient | NDC |
---|---|---|
Novel Laboratories Inc | moxifloxacin hydrochloride | 40032-034 |
Physicians Total Care Inc | moxifloxacin hydrochloride | 54868-4367 |
RedPharm Drug Inc | moxifloxacin hydrochloride | 67296-0154 |
RedPharm Drug Inc | moxifloxacin hydrochloride | 67296-1299 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing LACTOSE MONOHYDRATE
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
>Company | >Ingredient | >NDC |
Excipient focus: MAGNESIUM STEARATE
moxifloxacin hydrochloride drug variants containing MAGNESIUM STEARATE
moxifloxacin hydrochloride drug variants not containing MAGNESIUM STEARATE
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
Upsher-Smith Laboratories LLC | moxifloxacin hydrochloride | 0832-1410 |
>Company | >Ingredient | >NDC |
Excipient focus: MANNITOL
moxifloxacin hydrochloride drug variants containing MANNITOL
Company | Ingredient | NDC |
---|---|---|
Sunshine Lake Pharma Co Ltd | moxifloxacin hydrochloride | 48792-7823 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing MANNITOL
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
>Company | >Ingredient | >NDC |
Excipient focus: POLYETHYLENE GLYCOL
moxifloxacin hydrochloride drug variants containing POLYETHYLENE GLYCOL
moxifloxacin hydrochloride drug variants not containing POLYETHYLENE GLYCOL
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
>Company | >Ingredient | >NDC |
Excipient focus: POLYETHYLENE GLYCOL 400
moxifloxacin hydrochloride drug variants containing POLYETHYLENE GLYCOL 400
moxifloxacin hydrochloride drug variants not containing POLYETHYLENE GLYCOL 400
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
Upsher-Smith Laboratories LLC | moxifloxacin hydrochloride | 0832-1410 |
>Company | >Ingredient | >NDC |
Excipient focus: POLYETHYLENE GLYCOL 4000
moxifloxacin hydrochloride drug variants containing POLYETHYLENE GLYCOL 4000
Company | Ingredient | NDC |
---|---|---|
Major Pharmaceuticals | moxifloxacin hydrochloride | 0904-7407 |
A-S Medication Solutions | moxifloxacin hydrochloride | 50090-6595 |
A-S Medication Solutions | moxifloxacin hydrochloride | 50090-6609 |
A-S Medication Solutions | moxifloxacin hydrochloride | 50090-7244 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing POLYETHYLENE GLYCOL 4000
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
>Company | >Ingredient | >NDC |
Excipient focus: POLYVINYL ALCOHOL
moxifloxacin hydrochloride drug variants containing POLYVINYL ALCOHOL
moxifloxacin hydrochloride drug variants not containing POLYVINYL ALCOHOL
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
>Company | >Ingredient | >NDC |
Excipient focus: POVIDONE K30
moxifloxacin hydrochloride drug variants containing POVIDONE K30
moxifloxacin hydrochloride drug variants not containing POVIDONE K30
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
>Company | >Ingredient | >NDC |
Excipient focus: SILICON DIOXIDE
moxifloxacin hydrochloride drug variants containing SILICON DIOXIDE
moxifloxacin hydrochloride drug variants not containing SILICON DIOXIDE
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
Upsher-Smith Laboratories LLC | moxifloxacin hydrochloride | 0832-1410 |
>Company | >Ingredient | >NDC |
Excipient focus: SODIUM ACETATE
moxifloxacin hydrochloride drug variants containing SODIUM ACETATE
Company | Ingredient | NDC |
---|---|---|
Fresenius Kabi USA LLC | moxifloxacin hydrochloride | 63323-850 |
Fresenius Kabi Norge AS | moxifloxacin hydrochloride | 66298-8507 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing SODIUM ACETATE
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
>Company | >Ingredient | >NDC |
Excipient focus: SODIUM CHLORIDE
moxifloxacin hydrochloride drug variants containing SODIUM CHLORIDE
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
Upsher-Smith Laboratories LLC | moxifloxacin hydrochloride | 0832-1410 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing SODIUM CHLORIDE
Excipient focus: SODIUM HYDROXIDE
moxifloxacin hydrochloride drug variants containing SODIUM HYDROXIDE
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
Upsher-Smith Laboratories LLC | moxifloxacin hydrochloride | 0832-1410 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing SODIUM HYDROXIDE
Excipient focus: SODIUM STARCH GLYCOLATE TYPE A POTATO
moxifloxacin hydrochloride drug variants containing SODIUM STARCH GLYCOLATE TYPE A POTATO
Company | Ingredient | NDC |
---|---|---|
Major Pharmaceuticals | moxifloxacin hydrochloride | 0904-7407 |
A-S Medication Solutions | moxifloxacin hydrochloride | 50090-6595 |
A-S Medication Solutions | moxifloxacin hydrochloride | 50090-6609 |
A-S Medication Solutions | moxifloxacin hydrochloride | 50090-7244 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing SODIUM STARCH GLYCOLATE TYPE A POTATO
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
>Company | >Ingredient | >NDC |
Excipient focus: SODIUM SULFATE
moxifloxacin hydrochloride drug variants containing SODIUM SULFATE
Company | Ingredient | NDC |
---|---|---|
Fresenius Kabi USA LLC | moxifloxacin hydrochloride | 63323-850 |
Fresenius Kabi Norge AS | moxifloxacin hydrochloride | 66298-8507 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing SODIUM SULFATE
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
>Company | >Ingredient | >NDC |
Excipient focus: SORBITOL
moxifloxacin hydrochloride drug variants containing SORBITOL
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing SORBITOL
Excipient focus: STARCH, CORN
moxifloxacin hydrochloride drug variants containing STARCH, CORN
moxifloxacin hydrochloride drug variants not containing STARCH, CORN
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
>Company | >Ingredient | >NDC |
Excipient focus: SULFURIC ACID
moxifloxacin hydrochloride drug variants containing SULFURIC ACID
Company | Ingredient | NDC |
---|---|---|
Fresenius Kabi USA LLC | moxifloxacin hydrochloride | 63323-850 |
Fresenius Kabi Norge AS | moxifloxacin hydrochloride | 66298-8507 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing SULFURIC ACID
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Teva Pharmaceuticals USA Inc | moxifloxacin hydrochloride | 0093-7387 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
>Company | >Ingredient | >NDC |
Excipient focus: TALC
moxifloxacin hydrochloride drug variants containing TALC
moxifloxacin hydrochloride drug variants not containing TALC
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
Upsher-Smith Laboratories LLC | moxifloxacin hydrochloride | 0832-1410 |
>Company | >Ingredient | >NDC |
Excipient focus: TITANIUM DIOXIDE
moxifloxacin hydrochloride drug variants containing TITANIUM DIOXIDE
moxifloxacin hydrochloride drug variants not containing TITANIUM DIOXIDE
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
Upsher-Smith Laboratories LLC | moxifloxacin hydrochloride | 0832-1410 |
>Company | >Ingredient | >NDC |
Excipient focus: TYLOXAPOL
moxifloxacin hydrochloride drug variants containing TYLOXAPOL
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing TYLOXAPOL
Excipient focus: WATER
moxifloxacin hydrochloride drug variants containing WATER
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
Novartis Pharmaceuticals Corporation | moxifloxacin hydrochloride | 0078-0939 |
Sandoz Inc | moxifloxacin hydrochloride | 0781-7135 |
Upsher-Smith Laboratories LLC | moxifloxacin hydrochloride | 0832-1410 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing WATER
Excipient focus: XANTHAN GUM
moxifloxacin hydrochloride drug variants containing XANTHAN GUM
Company | Ingredient | NDC |
---|---|---|
Alcon Laboratories Inc | moxifloxacin hydrochloride | 0065-0006 |
>Company | >Ingredient | >NDC |
moxifloxacin hydrochloride drug variants not containing XANTHAN GUM
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