Package 59746-122-10

Brand: meclizine hydrochloride

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59746-122-10
Digits Only 5974612210
Product NDC 59746-122
Description

1000 TABLET in 1 BOTTLE (59746-122-10)

Marketing

Marketing Status
Discontinued 2026-10-31
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": "ead33f00-e158-464f-953f-ab5a9a391199", "openfda": {"upc": ["0359746121068", "0359746122065"], "unii": ["HDP7W44CIO"], "rxcui": ["995624", "995666"], "spl_set_id": ["9350fefc-9c00-182c-c3a9-044d4a40856f"], "manufacturer_name": ["Jubilant Cadista Pharmacuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59746-122-06)", "package_ndc": "59746-122-06", "marketing_end_date": "20261031", "marketing_start_date": "20100604"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (59746-122-10)", "package_ndc": "59746-122-10", "marketing_end_date": "20261031", "marketing_start_date": "20100604"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "59746-122_ead33f00-e158-464f-953f-ab5a9a391199", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "59746-122", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Jubilant Cadista Pharmacuticals Inc.", "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"}