Product NDC: | 0472-0912 |
Proprietary Name: | METRONIDAZOLE |
Non Proprietary Name: | METRONIDAZOLE LOTION 0.75% |
Active Ingredient(s): | 7.5 mg/g & nbsp; METRONIDAZOLE LOTION 0.75% |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0472-0912 |
Labeler Name: | Actavis Mid Atlantic LLC, Lincolnton, NC 28092 |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020901 |
Marketing Category: | NDA |
Start Marketing Date: | 20090528 |
Package NDC: | 0472-0912-02 |
Package Description: | 59.7 g in 1 BOTTLE, PLASTIC (0472-0912-02) |
NDC Code | 0472-0912-02 |
Proprietary Name | METRONIDAZOLE |
Package Description | 59.7 g in 1 BOTTLE, PLASTIC (0472-0912-02) |
Product NDC | 0472-0912 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | METRONIDAZOLE LOTION 0.75% |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20090528 |
Marketing Category Name | NDA |
Labeler Name | Actavis Mid Atlantic LLC, Lincolnton, NC 28092 |
Substance Name | METRONIDAZOLE |
Strength Number | 7.5 |
Strength Unit | mg/g |
Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |