Product NDC: | 0299-3820 |
Proprietary Name: | METROGEL |
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) |
Product NDC: | 0299-3820 |
Labeler Name: | Galderma Laboratories, L.P. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021789 |
Marketing Category: | NDA |
Start Marketing Date: | 20050630 |
Package NDC: | 0299-3820-01 |
Package Description: | 55 g in 1 BOTTLE, PUMP (0299-3820-01) |
NDC Code | 0299-3820-01 |
Proprietary Name | METROGEL |
Package Description | 55 g in 1 BOTTLE, PUMP (0299-3820-01) |
Product NDC | 0299-3820 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | metronidazole |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20050630 |
Marketing Category Name | NDA |
Labeler Name | Galderma Laboratories, L.P. |
Substance Name | METRONIDAZOLE |
Strength Number | 10 |
Strength Unit | mg/g |
Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |