Terbinex - Terbinafine Hydrochloride
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NDC Code: | 68712-037 |
Proprietary Name: | Terbinex |
Suffix: | |
Non-Proprietary Name: | Terbinafine Hydrochloride |
Dosage Form: | TABLET |
Method: | ORAL |
Original Marketing Date: | 31-01-2009 |
Category Name: | ANDA |
Application Number: | ANDA077533 |
Labeler: | INNOCUTIS |
Substance Name: | TERBINAFINE HYDROCHLORIDE |
Active Numerator Strength: | 250 |
Active Ingredient Unit: | mg/1 |
Pharm Classes: | Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC] |
DEA Schedule: |