FDA NDC Directory · JSON-LD · Markdown

Metoclopramide

NDC 60687-620 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA072801
Dosage form / routeTABLET · ORAL
Active ingredientsMETOCLOPRAMIDE HYDROCHLORIDE (5 mg/1)
Marketing started20211111
Package count1

External sources

Source: openFDA. Public-domain (CC0).