# Metoclopramide

NDC: 23155-240
Generic name: Metoclopramide Hydrochloride
Labeler / Manufacturer: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20140103

FDA application: ANDA204756

## Active ingredients

- METOCLOPRAMIDE HYDROCHLORIDE: 5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"23155-240"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-240
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=50a3cf38-66dc-4fa5-8a45-adf959c987ab