| Product NDC: | 68788-9887 |
| Proprietary Name: | Metronidazole |
| Non Proprietary Name: | metronidazole |
| Active Ingredient(s): | 7.5 mg/g & nbsp; metronidazole |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68788-9887 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020208 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20120214 |
| Package NDC: | 68788-9887-7 |
| Package Description: | 70 g in 1 TUBE, WITH APPLICATOR (68788-9887-7) |
| NDC Code | 68788-9887-7 |
| Proprietary Name | Metronidazole |
| Package Description | 70 g in 1 TUBE, WITH APPLICATOR (68788-9887-7) |
| Product NDC | 68788-9887 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | metronidazole |
| Dosage Form Name | GEL |
| Route Name | VAGINAL |
| Start Marketing Date | 20120214 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Preferred Pharmaceuticals, Inc |
| Substance Name | METRONIDAZOLE |
| Strength Number | 7.5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |