| NDC Code | 43063-906-90 |
|---|
| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (43063-906-90) |
|---|
| Product NDC | 43063-906 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Terbinafine Hydrochloride |
|---|
| Non-Proprietary Name | Terbinafine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20101227 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077714 |
|---|
| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
|---|
| Substance Name | TERBINAFINE HYDROCHLORIDE |
|---|
| Strength | 250 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Allylamine Antifungal [EPC], Allylamine [CS] |
|---|