Package 72162-1690-0

Brand: meclizine hydrochloride

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1690-0
Digits Only 7216216900
Product NDC 72162-1690
Product ID 72162-1690_42780752-9cd6-95e5-e063-6394a90abc0f
Description

1000 TABLET in 1 BOTTLE (72162-1690-0)

Marketing

Marketing Status
Discontinued 2026-10-31
Brand meclizine hydrochloride
Generic meclizine hydrochloride
Sample Package No

Linked Drug Pages (1)

MECLIZINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "42780752-9cd6-95e5-e063-6394a90abc0f", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624"], "spl_set_id": ["522b55a2-313c-45e8-b1be-07746ada5b0a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1690-0)", "package_ndc": "72162-1690-0", "marketing_end_date": "20261031", "marketing_start_date": "20230912"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "72162-1690_42780752-9cd6-95e5-e063-6394a90abc0f", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "72162-1690", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MECLIZINE HYDROCHLORIDE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA040659", "marketing_category": "ANDA", "marketing_end_date": "20261031", "marketing_start_date": "20100604"}