Product NDC: | 51672-4116 |
Proprietary Name: | Metronidazole |
Non Proprietary Name: | metronidazole |
Active Ingredient(s): | 7.5 mg/g & nbsp; metronidazole |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51672-4116 |
Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077819 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060718 |
Package NDC: | 51672-4116-5 |
Package Description: | 5 g in 1 TUBE (51672-4116-5) |
NDC Code | 51672-4116-5 |
Proprietary Name | Metronidazole |
Package Description | 5 g in 1 TUBE (51672-4116-5) |
Product NDC | 51672-4116 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | metronidazole |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20060718 |
Marketing Category Name | ANDA |
Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
Substance Name | METRONIDAZOLE |
Strength Number | 7.5 |
Strength Unit | mg/g |
Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |