Package 53746-441-10

Brand: meclizine hydrochloride

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 53746-441-10
Digits Only 5374644110
Product NDC 53746-441
Description

1000 TABLET in 1 BOTTLE (53746-441-10)

Marketing

Marketing Status
Marketed Since 2022-04-22
Brand meclizine hydrochloride
Generic meclizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d2a3b72-dab2-4e9f-b223-d6b591e2ed0c", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624", "995666"], "spl_set_id": ["ff719d9c-8d80-42db-97a5-022a75773623"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (53746-441-01)", "package_ndc": "53746-441-01", "marketing_start_date": "20220422"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (53746-441-10)", "package_ndc": "53746-441-10", "marketing_start_date": "20220422"}], "brand_name": "Meclizine Hydrochloride", "product_id": "53746-441_2d2a3b72-dab2-4e9f-b223-d6b591e2ed0c", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "53746-441", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA201451", "marketing_category": "ANDA", "marketing_start_date": "20220422", "listing_expiration_date": "20261231"}