# MECLIZINE HYDROCHLORIDE

NDC: 70518-1308
Generic name: Meclizine Hydrocloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180817
Marketing ended: 20261031
FDA application: ANDA040659

## Active ingredients

- MECLIZINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-1308"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-1308
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ba2fb6de-af86-4c05-9018-135e1f8594f9