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Noritate
Noritate - 0066-9850-60 - (metronidazole)
Drug Information of Noritate
| Product NDC: | 0066-9850 |
| Proprietary Name: | Noritate |
| Non Proprietary Name: | metronidazole |
| Active Ingredient(s): | 10 mg/60g & nbsp; metronidazole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Noritate
| Product NDC: | 0066-9850 |
| Labeler Name: | Dermik Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020743 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19970926 |
Package Information of Noritate
| Package NDC: | 0066-9850-60 |
| Package Description: | 60 g in 1 TUBE (0066-9850-60) |
NDC Information of Noritate
| NDC Code | 0066-9850-60 |
| Proprietary Name | Noritate |
| Package Description | 60 g in 1 TUBE (0066-9850-60) |
| Product NDC | 0066-9850 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | metronidazole |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19970926 |
| Marketing Category Name | NDA |
| Labeler Name | Dermik Laboratories |
| Substance Name | METRONIDAZOLE |
| Strength Number | 10 |
| Strength Unit | mg/60g |
| Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |
