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Metoclopramide

NDC 76045-213 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameMetoclopramide Hydrochloride
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA091392
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsMETOCLOPRAMIDE HYDROCHLORIDE (10 mg/2mL)
Marketing started20130503
Package count1

External sources

Source: openFDA. Public-domain (CC0).