Package 50268-522-15

Brand: meclizine hydrochloride

Generic: meclizine
NDC Package

Package Facts

Identity

Package NDC 50268-522-15
Digits Only 5026852215
Product NDC 50268-522
Product ID 50268-522_47e73600-a8db-31d6-e063-6294a90a47f3
Description

50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-522-15) / 1 TABLET in 1 BLISTER PACK (50268-522-11)

Marketing

Marketing Status
Marketed Since 2013-08-08
Brand meclizine hydrochloride
Generic meclizine
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": "47e73600-a8db-31d6-e063-6294a90a47f3", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624", "995666"], "spl_set_id": ["af5d0c9b-a997-8033-afca-3c04221f2e76"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-522-15)  / 1 TABLET in 1 BLISTER PACK (50268-522-11)", "package_ndc": "50268-522-15", "marketing_start_date": "20130808"}], "brand_name": "Meclizine Hydrochloride", "product_id": "50268-522_47e73600-a8db-31d6-e063-6294a90a47f3", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "50268-522", "generic_name": "Meclizine", "labeler_name": "AvPAK", "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": "20130808", "listing_expiration_date": "20271231"}