Product NDC: | 0168-0323 |
Proprietary Name: | Metronidazole |
Non Proprietary Name: | Metronidazole |
Active Ingredient(s): | 7.5 mg/g & nbsp; Metronidazole |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0168-0323 |
Labeler Name: | E.FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076408 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040528 |
Package NDC: | 0168-0323-46 |
Package Description: | 45 g in 1 TUBE (0168-0323-46) |
NDC Code | 0168-0323-46 |
Proprietary Name | Metronidazole |
Package Description | 45 g in 1 TUBE (0168-0323-46) |
Product NDC | 0168-0323 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Metronidazole |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20040528 |
Marketing Category Name | ANDA |
Labeler Name | E.FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. |
Substance Name | METRONIDAZOLE |
Strength Number | 7.5 |
Strength Unit | mg/g |
Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |