Product NDC: | 29336-200 |
Proprietary Name: | MetroGel-Vaginal |
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: | 29336-200 |
Labeler Name: | Graceway Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020014 |
Marketing Category: | NDA |
Start Marketing Date: | 20100101 |
Package NDC: | 29336-200-25 |
Package Description: | 70 g in 1 TUBE, WITH APPLICATOR (29336-200-25) |
NDC Code | 29336-200-25 |
Proprietary Name | MetroGel-Vaginal |
Package Description | 70 g in 1 TUBE, WITH APPLICATOR (29336-200-25) |
Product NDC | 29336-200 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | metronidazole |
Dosage Form Name | GEL |
Route Name | VAGINAL |
Start Marketing Date | 20100101 |
Marketing Category Name | NDA |
Labeler Name | Graceway Pharmaceuticals, LLC |
Substance Name | METRONIDAZOLE |
Strength Number | 7.5 |
Strength Unit | mg/g |
Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |