| Product NDC: | 66993-935 |
| 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: | 66993-935 |
| Labeler Name: | Prasco Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020208 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20070331 |
| Package NDC: | 66993-935-70 |
| Package Description: | 70 g in 1 TUBE, WITH APPLICATOR (66993-935-70) |
| NDC Code | 66993-935-70 |
| Proprietary Name | Metronidazole |
| Package Description | 70 g in 1 TUBE, WITH APPLICATOR (66993-935-70) |
| Product NDC | 66993-935 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | metronidazole |
| Dosage Form Name | GEL |
| Route Name | VAGINAL |
| Start Marketing Date | 20070331 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Prasco Laboratories |
| Substance Name | METRONIDAZOLE |
| Strength Number | 7.5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |