NDC Code | 55111-250-79 |
Package Description | 10 BLISTER PACK in 1 CARTON (55111-250-79) > 10 TABLET in 1 BLISTER PACK (55111-250-78) |
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] |