Product NDC: | 60760-334 |
Proprietary Name: | METRONIDAZOLE |
Non Proprietary Name: | METRONIDAZOLE |
Active Ingredient(s): | 500 mg/1 & nbsp; METRONIDAZOLE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60760-334 |
Labeler Name: | St Marys Medical Park Pharmacy |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA070033 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130110 |
Package NDC: | 60760-334-14 |
Package Description: | 14 TABLET in 1 BOTTLE, PLASTIC (60760-334-14) |
NDC Code | 60760-334-14 |
Proprietary Name | METRONIDAZOLE |
Package Description | 14 TABLET in 1 BOTTLE, PLASTIC (60760-334-14) |
Product NDC | 60760-334 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | METRONIDAZOLE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20130110 |
Marketing Category Name | ANDA |
Labeler Name | St Marys Medical Park Pharmacy |
Substance Name | METRONIDAZOLE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |