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Terbinex
Terbinex - 68712-037-01 - (Terbinafine Hydrochloride)
Drug Information of Terbinex
| Product NDC: | 68712-037 |
| Proprietary Name: | Terbinex |
| 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 Terbinex
| Product NDC: | 68712-037 |
| Labeler Name: | Innocutis |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077533 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090131 |
Package Information of Terbinex
| Package NDC: | 68712-037-01 |
| Package Description: | 42 TABLET in 1 BOTTLE, PLASTIC (68712-037-01) |
NDC Information of Terbinex
| NDC Code | 68712-037-01 |
| Proprietary Name | Terbinex |
| Package Description | 42 TABLET in 1 BOTTLE, PLASTIC (68712-037-01) |
| Product NDC | 68712-037 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Terbinafine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090131 |
| Marketing Category Name | ANDA |
| Labeler Name | Innocutis |
| Substance Name | TERBINAFINE HYDROCHLORIDE |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC] |
