| Product NDC: | 0338-1055 | 
| 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: | 0338-1055 | 
| Labeler Name: | Baxter Healthcare Corporation | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | NDA018657 | 
| Marketing Category: | NDA | 
| Start Marketing Date: | 19811224 | 
| Package NDC: | 0338-1055-48 | 
| Package Description: | 24 BAG in 1 CARTON (0338-1055-48) > 100 mL in 1 BAG | 
| NDC Code | 0338-1055-48 | 
| Proprietary Name | Metronidazole | 
| Package Description | 24 BAG in 1 CARTON (0338-1055-48) > 100 mL in 1 BAG | 
| Product NDC | 0338-1055 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Metronidazole | 
| Dosage Form Name | INJECTION, SOLUTION | 
| Route Name | INTRAVENOUS | 
| Start Marketing Date | 19811224 | 
| Marketing Category Name | NDA | 
| Labeler Name | Baxter Healthcare Corporation | 
| Substance Name | METRONIDAZOLE | 
| Strength Number | 500 | 
| Strength Unit | mg/100mL | 
| Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |