Product NDC: | 36000-028 |
Proprietary Name: | METRONIDAZOLE |
Non Proprietary Name: | METRONIDAZOLE |
Active Ingredient(s): | 500 mg/100mL & nbsp; METRONIDAZOLE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 36000-028 |
Labeler Name: | Claris Lifesciences Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078084 |
Marketing Category: | ANDA |
Start Marketing Date: | 20081120 |
Package NDC: | 36000-028-24 |
Package Description: | 1 BAG in 1 CARTON (36000-028-24) > 100 mL in 1 BAG |
NDC Code | 36000-028-24 |
Proprietary Name | METRONIDAZOLE |
Package Description | 1 BAG in 1 CARTON (36000-028-24) > 100 mL in 1 BAG |
Product NDC | 36000-028 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | METRONIDAZOLE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20081120 |
Marketing Category Name | ANDA |
Labeler Name | Claris Lifesciences Inc. |
Substance Name | METRONIDAZOLE |
Strength Number | 500 |
Strength Unit | mg/100mL |
Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |