Package 0904-7375-61

Brand: meclizine hydrochloride

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7375-61
Digits Only 0904737561
Product NDC 0904-7375
Product ID 0904-7375_87ac0ee9-aa64-4037-a047-a6d3a81da8d2
Description

100 BLISTER PACK in 1 CARTON (0904-7375-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2023-07-18
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": "87ac0ee9-aa64-4037-a047-a6d3a81da8d2", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624", "995666"], "spl_set_id": ["f99f13ab-33c0-4304-8dc5-3a75f3909377"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7375-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7375-61", "marketing_start_date": "20230718"}], "brand_name": "Meclizine Hydrochloride", "product_id": "0904-7375_87ac0ee9-aa64-4037-a047-a6d3a81da8d2", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "0904-7375", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "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"}