NDC 70700-161
Naftifine hydrochloride
Naftifine Hydrochloride
Naftifine hydrochloride is a Topical Cream in the Human Prescription Drug category. It is labeled and distributed by Xiromed, Llc. The primary component is Naftifine Hydrochloride.
| Product ID | 70700-161_7ad13433-2f93-1881-5fe6-2e0630ac70fe |
| NDC | 70700-161 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Naftifine hydrochloride |
| Generic Name | Naftifine Hydrochloride |
| Dosage Form | Cream |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2021-01-15 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA210038 |
| Labeler Name | Xiromed, LLC |
| Substance Name | NAFTIFINE HYDROCHLORIDE |
| Active Ingredient Strength | 20 mg/g |
| Pharm Classes | Allylamine [CS],Allylamine Antifungal [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |