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Metronidazole
Metronidazole - 0781-7080-55 - (Metronidazole)
Drug Information of Metronidazole
| Product NDC: | 0781-7080 |
| Proprietary Name: | Metronidazole |
| Non Proprietary Name: | Metronidazole |
| Active Ingredient(s): | 10 mg/g & nbsp; Metronidazole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metronidazole
| Product NDC: | 0781-7080 |
| Labeler Name: | Sandoz Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090903 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130701 |
Package Information of Metronidazole
| Package NDC: | 0781-7080-55 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (0781-7080-55) > 55 g in 1 BOTTLE, PUMP |
NDC Information of Metronidazole
| NDC Code | 0781-7080-55 |
| Proprietary Name | Metronidazole |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (0781-7080-55) > 55 g in 1 BOTTLE, PUMP |
| Product NDC | 0781-7080 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metronidazole |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20130701 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc. |
| Substance Name | METRONIDAZOLE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |
