Naftifine Hydrochloride is a Topical Gel in the Human Prescription Drug category. It is labeled and distributed by Taro Pharmaceuticals U.s.a., Inc.. The primary component is Naftifine Hydrochloride.
Product ID | 51672-1376_1d371d0c-4648-4c2f-992f-2c6c99040474 |
NDC | 51672-1376 |
Product Type | Human Prescription Drug |
Proprietary Name | Naftifine Hydrochloride |
Generic Name | Naftifine Hydrochloride |
Dosage Form | Gel |
Route of Administration | TOPICAL |
Marketing Start Date | 2019-04-10 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA208201 |
Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
Substance Name | NAFTIFINE HYDROCHLORIDE |
Active Ingredient Strength | 20 mg/g |
Pharm Classes | Allylamine [CS],Allylamine Antifungal [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2019-10-28 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA208201 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-10-28 |
Marketing Category | ANDA |
Application Number | ANDA208201 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-04-10 |
Ingredient | Strength |
---|---|
NAFTIFINE HYDROCHLORIDE | 20 mg/g |
NDC | Brand Name | Generic Name |
---|---|---|
0115-1510 | NAFTIFINE HYDROCHLORIDE | NAFTIFINE HYDROCHLORIDE |
0115-1512 | NAFTIFINE HYDROCHLORIDE | NAFTIFINE HYDROCHLORIDE |
40085-201 | Naftifine Hydrochloride | NAFTIFINE HYDROCHLORIDE |
40085-203 | Naftifine Hydrochloride | NAFTIFINE HYDROCHLORIDE |
51672-1362 | Naftifine Hydrochloride | Naftifine Hydrochloride |
51672-1368 | Naftifine Hydrochloride | Naftifine Hydrochloride |
51672-1376 | Naftifine Hydrochloride | Naftifine Hydrochloride |
70700-161 | Naftifine hydrochloride | Naftifine hydrochloride |
0259-4126 | Naftin | NAFTIFINE HYDROCHLORIDE |
54766-102 | Naftin | Naftifine Hydrochloride |
54766-770 | Naftin | NAFTIFINE HYDROCHLORIDE |
54766-772 | Naftin | Naftifine Hydrochloride |