# Meclizine Hydrochloride

NDC: 50090-5727
Generic name: Meclizine Hydrochloride
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20201029

FDA application: ANDA213957

## Active ingredients

- MECLIZINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-5727"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-5727
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=51c96c7a-0a38-41a5-a6c9-7f45db65fdda