Product NDC: | 0409-3506 |
Proprietary Name: | Meropenem |
Non Proprietary Name: | Meropenem |
Active Ingredient(s): | 1 g/20mL & nbsp; Meropenem |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-3506 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090940 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100623 |
Package NDC: | 0409-3506-01 |
Package Description: | 25 VIAL in 1 CARTON (0409-3506-01) > 20 mL in 1 VIAL |
NDC Code | 0409-3506-01 |
Proprietary Name | Meropenem |
Package Description | 25 VIAL in 1 CARTON (0409-3506-01) > 20 mL in 1 VIAL |
Product NDC | 0409-3506 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Meropenem |
Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100623 |
Marketing Category Name | ANDA |
Labeler Name | Hospira, Inc. |
Substance Name | MEROPENEM |
Strength Number | 1 |
Strength Unit | g/20mL |
Pharmaceutical Classes | Carbapenems [Chemical/Ingredient],Penem Antibacterial [EPC] |