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Metoclopramide

NDC 48433-066 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSafecor Health LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA072801
Dosage form / routeTABLET · ORAL
Active ingredientsMETOCLOPRAMIDE HYDROCHLORIDE (5 mg/1)
Marketing started20260403
Package count1

External sources

Source: openFDA. Public-domain (CC0).