| NDC Code | 0093-7294-56 |
|---|
| Package Description | 30 TABLET in 1 BOTTLE (0093-7294-56) |
|---|
| Product NDC | 0093-7294 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Terbinafine Hydrochloride |
|---|
| Non-Proprietary Name | Terbinafine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20070703 |
|---|
| End Marketing Date | 20140228 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076377 |
|---|
| Manufacturer | Teva Pharmaceuticals USA Inc |
|---|
| Substance Name | TERBINAFINE HYDROCHLORIDE |
|---|
| Strength | 250 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC] |
|---|