Product NDC: | 0299-3836 |
Proprietary Name: | MetroCream |
Non Proprietary Name: | metronidazole |
Active Ingredient(s): | 7.5 mg/g & nbsp; metronidazole |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0299-3836 |
Labeler Name: | Galderma Laboratories, L.P. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020531 |
Marketing Category: | NDA |
Start Marketing Date: | 19950920 |
Package NDC: | 0299-3836-45 |
Package Description: | 1 TUBE in 1 CARTON (0299-3836-45) > 45 g in 1 TUBE |
NDC Code | 0299-3836-45 |
Proprietary Name | MetroCream |
Package Description | 1 TUBE in 1 CARTON (0299-3836-45) > 45 g in 1 TUBE |
Product NDC | 0299-3836 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | metronidazole |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19950920 |
Marketing Category Name | NDA |
Labeler Name | Galderma Laboratories, L.P. |
Substance Name | METRONIDAZOLE |
Strength Number | 7.5 |
Strength Unit | mg/g |
Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |