Package 80513-427-02

Brand: meclizine

Generic: meclizine hcl 12.5 mg
NDC Package

Package Facts

Identity

Package NDC 80513-427-02
Digits Only 8051342702
Product NDC 80513-427
Product ID 80513-427_3e5a4128-ff9c-6f2b-e063-6394a90a42e6
Description

200 TABLET in 1 BOTTLE, PLASTIC (80513-427-02)

Marketing

Marketing Status
Marketed Since 2025-09-01
Brand meclizine
Generic meclizine hcl 12.5 mg
Sample Package No

Linked Drug Pages (1)

MECLIZINE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e5a4128-ff9c-6f2b-e063-6394a90a42e6", "openfda": {"upc": ["0380513000316"], "unii": ["HDP7W44CIO"], "rxcui": ["995624"], "spl_set_id": ["032a89f2-17e7-45d2-94a1-cc7a601ebdee"], "manufacturer_name": ["Advanced Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE, PLASTIC (80513-427-02)", "package_ndc": "80513-427-02", "marketing_start_date": "20250901"}], "brand_name": "MECLIZINE", "product_id": "80513-427_3e5a4128-ff9c-6f2b-e063-6394a90a42e6", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "80513-427", "generic_name": "Meclizine HCl 12.5 mg", "labeler_name": "Advanced Rx LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MECLIZINE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250901", "listing_expiration_date": "20261231"}