# Metoclopramide

NDC: 76045-213
Generic name: Metoclopramide Hydrochloride
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20130503

FDA application: ANDA091392

## Active ingredients

- METOCLOPRAMIDE HYDROCHLORIDE: 10 mg/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76045-213"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76045-213
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cc739885-e10e-4bcb-a781-c726c518f3d1