Product NDC: | 0143-9772 |
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: | 0143-9772 |
Labeler Name: | West-ward Pharmaceutical Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078084 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090804 |
Package NDC: | 0143-9772-26 |
Package Description: | 100 mL in 1 BAG (0143-9772-26) |
NDC Code | 0143-9772-26 |
Proprietary Name | Metronidazole |
Package Description | 100 mL in 1 BAG (0143-9772-26) |
Product NDC | 0143-9772 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Metronidazole |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20090804 |
Marketing Category Name | ANDA |
Labeler Name | West-ward Pharmaceutical Corp |
Substance Name | METRONIDAZOLE |
Strength Number | 500 |
Strength Unit | mg/100mL |
Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |