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Metoclopramide

NDC 63187-235 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA070184
Dosage form / routeTABLET · ORAL
Active ingredientsMETOCLOPRAMIDE HYDROCHLORIDE (10 mg/1)
Marketing started19900930
Package count4

External sources

Source: openFDA. Public-domain (CC0).