# MECLIZINE HYDROCHLORIDE

NDC: 60760-997
Generic name: MECLIZINE
Labeler / Manufacturer: St. Mary's Medical Park Pharmacy
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20261006

FDA application: ANDA202640

## Active ingredients

- MECLIZINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60760-997"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60760-997