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NDC 51672-2083-08 Terbinafine Hydrochloride 1 g/100g Details
Terbinafine Hydrochloride 1 g/100g
Terbinafine Hydrochloride is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by Taro Pharmaceuticals U.S.A., Inc.. The primary component is TERBINAFINE HYDROCHLORIDE.
Product Information
| NDC | 51672-2083 |
|---|---|
| Product ID | 51672-2083_369cabfd-6c6a-40b4-b3d7-45a871b9964c |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Terbinafine Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Terbinafine Hydrochloride |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | CREAM |
| Route | TOPICAL |
| Active Ingredient Strength | 1 |
| Active Ingredient Units | g/100g |
| Substance Name | TERBINAFINE HYDROCHLORIDE |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Pharmaceutical Class | Allylamine Antifungal [EPC], Allylamine [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA077511 |
| Listing Certified Through | 2023-12-31 |
Package
NDC 51672-2083-08 (51672208308)
| NDC Package Code | 51672-2083-8 |
|---|---|
| Billing NDC | 51672208308 |
| Package | 1 TUBE in 1 CARTON (51672-2083-8) / 12 g in 1 TUBE |
| Marketing Start Date | 2007-07-02 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |