| NDC Code | 55111-250-05 |
|---|
| Package Description | 500 TABLET in 1 BOTTLE (55111-250-05) |
|---|
| Product NDC | 55111-250 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Terbinafine Hydrochloride |
|---|
| Non-Proprietary Name | Terbinafine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20070702 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076390 |
|---|
| Manufacturer | Dr.Reddys Laboratories Limited |
|---|
| Substance Name | TERBINAFINE HYDROCHLORIDE |
|---|
| Strength | 250 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Allylamine Antifungal [EPC], Allylamine [CS] |
|---|