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Meropenem

NDC 0409-0222 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerHospira, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091404
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsMEROPENEM (500 mg/10mL)
Marketing started20221206
Package count1

External sources

Source: openFDA. Public-domain (CC0).