Product NDC: | 63323-507 |
Proprietary Name: | Meropenem |
Non Proprietary Name: | Meropenem |
Active Ingredient(s): | 500 mg/10mL & nbsp; Meropenem |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63323-507 |
Labeler Name: | APP Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA091404 |
Marketing Category: | ANDA |
Start Marketing Date: | 20111014 |
Package NDC: | 63323-507-20 |
Package Description: | 10 VIAL in 1 CARTON (63323-507-20) > 10 mL in 1 VIAL |
NDC Code | 63323-507-20 |
Proprietary Name | Meropenem |
Package Description | 10 VIAL in 1 CARTON (63323-507-20) > 10 mL in 1 VIAL |
Product NDC | 63323-507 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Meropenem |
Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20111014 |
Marketing Category Name | ANDA |
Labeler Name | APP Pharmaceuticals, LLC |
Substance Name | MEROPENEM |
Strength Number | 500 |
Strength Unit | mg/10mL |
Pharmaceutical Classes | Carbapenems [Chemical/Ingredient],Penem Antibacterial [EPC] |