Details for New Drug Application (NDA): 212616
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The generic ingredient in MOXIFLOXACIN HYDROCHLORIDE is moxifloxacin hydrochloride. There are eighteen drug master file entries for this compound. Thirty-five suppliers are listed for this compound. Additional details are available on the moxifloxacin hydrochloride profile page.
Summary for 212616
Tradename: | MOXIFLOXACIN HYDROCHLORIDE |
Applicant: | Upsher Smith Labs |
Ingredient: | moxifloxacin hydrochloride |
Patents: | 0 |
Suppliers and Packaging for NDA: 212616
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
MOXIFLOXACIN HYDROCHLORIDE | moxifloxacin hydrochloride | SOLUTION/DROPS;OPHTHALMIC | 212616 | ANDA | Upsher-Smith Laboratories, LLC | 0832-1410 | 0832-1410-03 | 1 BOTTLE, PLASTIC in 1 CARTON (0832-1410-03) / 3 mL in 1 BOTTLE, PLASTIC |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION/DROPS;OPHTHALMIC | Strength | EQ 0.5% BASE | ||||
Approval Date: | Feb 10, 2021 | TE: | AT1 | RLD: | No |
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