List of Excipients in API buprenorphine hcl
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Excipients in ANDA-approved (generic) drugs containing buprenorphine hcl
| Company | Ingredient | NDC | Excipient |
|---|---|---|---|
| Hikma Pharmaceuticals USA Inc | buprenorphine hcl | 0054-0176 | ANHYDROUS CITRIC ACID |
| Hikma Pharmaceuticals USA Inc | buprenorphine hcl | 0054-0176 | CROSPOVIDONE |
| Hikma Pharmaceuticals USA Inc | buprenorphine hcl | 0054-0176 | LACTOSE MONOHYDRATE |
| Hikma Pharmaceuticals USA Inc | buprenorphine hcl | 0054-0176 | MAGNESIUM STEARATE |
| Hikma Pharmaceuticals USA Inc | buprenorphine hcl | 0054-0176 | MANNITOL |
| >Company | >Ingredient | >NDC | >Excipient |
Detailed excipient profiles for buprenorphine hcl
Excipient focus: ANHYDROUS CITRIC ACID
buprenorphine hcl drug variants containing ANHYDROUS CITRIC ACID
buprenorphine hcl drug variants not containing ANHYDROUS CITRIC ACID
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: CROSPOVIDONE
buprenorphine hcl drug variants containing CROSPOVIDONE
buprenorphine hcl drug variants not containing CROSPOVIDONE
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: LACTOSE MONOHYDRATE
buprenorphine hcl drug variants containing LACTOSE MONOHYDRATE
buprenorphine hcl drug variants not containing LACTOSE MONOHYDRATE
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: MAGNESIUM STEARATE
buprenorphine hcl drug variants containing MAGNESIUM STEARATE
buprenorphine hcl drug variants not containing MAGNESIUM STEARATE
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: MANNITOL
buprenorphine hcl drug variants containing MANNITOL
buprenorphine hcl drug variants not containing MANNITOL
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: POVIDONE
buprenorphine hcl drug variants containing POVIDONE
buprenorphine hcl drug variants not containing POVIDONE
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: SODIUM CITRATE
buprenorphine hcl drug variants containing SODIUM CITRATE
buprenorphine hcl drug variants not containing SODIUM CITRATE
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: STARCH, CORN
buprenorphine hcl drug variants containing STARCH, CORN
buprenorphine hcl drug variants not containing STARCH, CORN
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: WATER
buprenorphine hcl drug variants containing WATER
buprenorphine hcl drug variants not containing WATER
| Company | Ingredient | NDC |
|---|---|---|
| Lake Erie Medical DBA Quality Care Products LLC | buprenorphine hcl | 55700-302 |
| >Company | >Ingredient | >NDC |
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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.
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