FDA NDC Directory · JSON-LD · Markdown

Meropenem

NDC 68001-323 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA205883
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsMEROPENEM (500 mg/20mL)
Marketing started20170430
Package count0

External sources

Source: openFDA. Public-domain (CC0).