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] |