| Product NDC: | 54868-5882 |
| Proprietary Name: | Metronidazole |
| Non Proprietary Name: | Metronidazole |
| Active Ingredient(s): | 7.5 mg/mL & nbsp; Metronidazole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54868-5882 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077197 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080327 |
| Package NDC: | 54868-5882-0 |
| Package Description: | 59 mL in 1 BOTTLE, PLASTIC (54868-5882-0) |
| NDC Code | 54868-5882-0 |
| Proprietary Name | Metronidazole |
| Package Description | 59 mL in 1 BOTTLE, PLASTIC (54868-5882-0) |
| Product NDC | 54868-5882 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metronidazole |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20080327 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | METRONIDAZOLE |
| Strength Number | 7.5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |