Product NDC: | 0409-7811 |
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: | 0409-7811 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018890 |
Marketing Category: | NDA |
Start Marketing Date: | 19831118 |
Package NDC: | 0409-7811-24 |
Package Description: | 24 POUCH in 1 CASE (0409-7811-24) > 1 POUCH in 1 POUCH > 100 mL in 1 POUCH |
NDC Code | 0409-7811-24 |
Proprietary Name | Metronidazole |
Package Description | 24 POUCH in 1 CASE (0409-7811-24) > 1 POUCH in 1 POUCH > 100 mL in 1 POUCH |
Product NDC | 0409-7811 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | METRONIDAZOLE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19831118 |
Marketing Category Name | NDA |
Labeler Name | Hospira, Inc. |
Substance Name | METRONIDAZOLE |
Strength Number | 500 |
Strength Unit | mg/100mL |
Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |