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Terbinafine
Terbinafine - 65862-079-01 - (Terbinafine Hydrochloride)
Drug Information of Terbinafine
| Product NDC: | 65862-079 |
| Proprietary Name: | Terbinafine |
| Non Proprietary Name: | Terbinafine Hydrochloride |
| Active Ingredient(s): | 250 mg/1 & nbsp; Terbinafine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Terbinafine
| Product NDC: | 65862-079 |
| Labeler Name: | Aurobindo Pharma Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078297 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070702 |
Package Information of Terbinafine
| Package NDC: | 65862-079-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (65862-079-01) |
NDC Information of Terbinafine
| NDC Code | 65862-079-01 |
| Proprietary Name | Terbinafine |
| Package Description | 100 TABLET in 1 BOTTLE (65862-079-01) |
| Product NDC | 65862-079 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Terbinafine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070702 |
| Marketing Category Name | ANDA |
| Labeler Name | Aurobindo Pharma Limited |
| Substance Name | TERBINAFINE HYDROCHLORIDE |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC] |
