Product NDC: | 68788-9814 |
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) |
Product NDC: | 68788-9814 |
Labeler Name: | Preferred Pharmaceuticals, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA077511 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120405 |
Package NDC: | 68788-9814-1 |
Package Description: | 15 g in 1 TUBE (68788-9814-1) |
NDC Code | 68788-9814-1 |
Proprietary Name | Terbinafine Hydrochloride |
Package Description | 15 g in 1 TUBE (68788-9814-1) |
Product NDC | 68788-9814 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Terbinafine Hydrochloride |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120405 |
Marketing Category Name | ANDA |
Labeler Name | Preferred Pharmaceuticals, Inc |
Substance Name | TERBINAFINE HYDROCHLORIDE |
Strength Number | 1 |
Strength Unit | g/100g |
Pharmaceutical Classes |