# Metoclopramide

NDC: 60687-631
Generic name: Metoclopramide
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220124

FDA application: ANDA070184

## Active ingredients

- METOCLOPRAMIDE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-631"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-631
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=998f1782-bbfa-469b-9fe1-c612e8588f70