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METRONIDAZOLE
METRONIDAZOLE - 36000-001-24 - (METRONIDAZOLE)
Drug Information of METRONIDAZOLE
| Product NDC: | 36000-001 |
| 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) |
Labeler Information of METRONIDAZOLE
| Product NDC: | 36000-001 |
| Labeler Name: | Claris Lifesciences Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078084 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081120 |
Package Information of METRONIDAZOLE
| Package NDC: | 36000-001-24 |
| Package Description: | 24 BAG in 1 CARTON (36000-001-24) > 100 mL in 1 BAG |
NDC Information of METRONIDAZOLE
| NDC Code | 36000-001-24 |
| Proprietary Name | METRONIDAZOLE |
| Package Description | 24 BAG in 1 CARTON (36000-001-24) > 100 mL in 1 BAG |
| Product NDC | 36000-001 |
| 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] |
