Meropenem - 63323-508-31 - (Meropenem)

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Drug Information of Meropenem

Product NDC: 63323-508
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)

Labeler Information of Meropenem

Product NDC: 63323-508
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091404
Marketing Category: ANDA
Start Marketing Date: 20111026

Package Information of Meropenem

Package NDC: 63323-508-31
Package Description: 10 VIAL in 1 CARTON (63323-508-31) > 20 mL in 1 VIAL

NDC Information of Meropenem

NDC Code 63323-508-31
Proprietary Name Meropenem
Package Description 10 VIAL in 1 CARTON (63323-508-31) > 20 mL in 1 VIAL
Product NDC 63323-508
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meropenem
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20111026
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name MEROPENEM
Strength Number 1
Strength Unit g/20mL
Pharmaceutical Classes Carbapenems [Chemical/Ingredient],Penem Antibacterial [EPC]

Complete Information of Meropenem


General Information