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] |