FDA NDC Directory · JSON-LD · Markdown

Imipenem and Cilastatin

NDC 63323-322 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Generic nameImipenem and Cilastatin Sodium
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090577
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsCILASTATIN SODIUM (500 mg/20mL)
IMIPENEM (500 mg/20mL)
Marketing started20120103
Package count1

External sources

Source: openFDA. Public-domain (CC0).