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Terbinafine Hydrochloride
Terbinafine Hydrochloride - 51672-2080-1 - (Terbinafine Hydrochloride)
Drug Information of Terbinafine Hydrochloride
| Product NDC: | 51672-2080 |
| Proprietary Name: | Terbinafine Hydrochloride |
| Non Proprietary Name: | Terbinafine Hydrochloride |
| Active Ingredient(s): | 1 g/100g & nbsp; Terbinafine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Terbinafine Hydrochloride
| Product NDC: | 51672-2080 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077511 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070702 |
Package Information of Terbinafine Hydrochloride
| Package NDC: | 51672-2080-1 |
| Package Description: | 1 TUBE in 1 CARTON (51672-2080-1) > 15 g in 1 TUBE |
NDC Information of Terbinafine Hydrochloride
| NDC Code | 51672-2080-1 |
| Proprietary Name | Terbinafine Hydrochloride |
| Package Description | 1 TUBE in 1 CARTON (51672-2080-1) > 15 g in 1 TUBE |
| Product NDC | 51672-2080 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Terbinafine Hydrochloride |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20070702 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | TERBINAFINE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
