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METOCLOPRAMIDE

NDC 51662-1288 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA073118
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsMETOCLOPRAMIDE HYDROCHLORIDE (5 mg/mL)
Marketing started20180922
Package count2

External sources

Source: openFDA. Public-domain (CC0).