Product NDC: | 0168-0383 |
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: | 0168-0383 |
Labeler Name: | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077197 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060524 |
Package NDC: | 0168-0383-60 |
Package Description: | 59 mL in 1 BOTTLE, PLASTIC (0168-0383-60) |
NDC Code | 0168-0383-60 |
Proprietary Name | Metronidazole |
Package Description | 59 mL in 1 BOTTLE, PLASTIC (0168-0383-60) |
Product NDC | 0168-0383 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Metronidazole |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20060524 |
Marketing Category Name | ANDA |
Labeler Name | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. |
Substance Name | METRONIDAZOLE |
Strength Number | 7.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |