Package 80513-421-02

Brand: meclizine

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 80513-421-02
Digits Only 8051342102
Product NDC 80513-421
Product ID 80513-421_27e17bc9-1e66-cc1f-e063-6394a90a4dcb
Description

200 TABLET, CHEWABLE in 1 BOTTLE (80513-421-02)

Marketing

Marketing Status
Marketed Since 2024-12-01
Brand meclizine
Generic meclizine hydrochloride
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": "27e17bc9-1e66-cc1f-e063-6394a90a4dcb", "openfda": {"upc": ["0380513000316"], "unii": ["HDP7W44CIO"], "rxcui": ["995632"], "spl_set_id": ["b0a2a1f7-354e-48bd-9e98-9207bf9f53fd"], "manufacturer_name": ["Advanced Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET, CHEWABLE in 1 BOTTLE (80513-421-02)", "package_ndc": "80513-421-02", "marketing_start_date": "20241201"}], "brand_name": "Meclizine", "product_id": "80513-421_27e17bc9-1e66-cc1f-e063-6394a90a4dcb", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "80513-421", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Advanced Rx LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Meclizine", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241201", "listing_expiration_date": "20261231"}