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MetroLotion
MetroLotion - 0299-3838-02 - (metronidazole)
Drug Information of MetroLotion
| Product NDC: | 0299-3838 |
| Proprietary Name: | MetroLotion |
| Non Proprietary Name: | metronidazole |
| Active Ingredient(s): | 7.5 mg/g & nbsp; metronidazole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MetroLotion
| Product NDC: | 0299-3838 |
| Labeler Name: | Galderma Laboratories, L.P. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020901 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19981124 |
Package Information of MetroLotion
| Package NDC: | 0299-3838-02 |
| Package Description: | 59.7 g in 1 BOTTLE, PLASTIC (0299-3838-02) |
NDC Information of MetroLotion
| NDC Code | 0299-3838-02 |
| Proprietary Name | MetroLotion |
| Package Description | 59.7 g in 1 BOTTLE, PLASTIC (0299-3838-02) |
| Product NDC | 0299-3838 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | metronidazole |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19981124 |
| 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] |
