# Metoclopramide

NDC: 0121-0576
Generic name: metoclopramide hydrochloride
Labeler / Manufacturer: PAI Holdings, LLC dba PAI Pharma
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 19910601

FDA application: ANDA072744

## Active ingredients

- METOCLOPRAMIDE HYDROCHLORIDE: 5 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0121-0576"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0121-0576
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3cc8ca5b-8b71-4c77-a181-9ce154597b9a