Package 42806-014-10

Brand: meclizine hydrochloride

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-014-10
Digits Only 4280601410
Product NDC 42806-014
Product ID 42806-014_42600718-075b-481b-8fec-cb6cbadab7de
Description

1000 TABLET in 1 BOTTLE (42806-014-10)

Marketing

Marketing Status
Marketed Since 2012-04-30
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": "42600718-075b-481b-8fec-cb6cbadab7de", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624", "995666"], "spl_set_id": ["467e464b-bbaf-4053-9136-39e47a92fa05"], "manufacturer_name": ["Epic Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42806-014-01)", "package_ndc": "42806-014-01", "marketing_start_date": "20120430"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (42806-014-10)", "package_ndc": "42806-014-10", "marketing_start_date": "20120430"}], "brand_name": "Meclizine Hydrochloride", "product_id": "42806-014_42600718-075b-481b-8fec-cb6cbadab7de", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "42806-014", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Epic Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA200294", "marketing_category": "ANDA", "marketing_start_date": "20120430", "listing_expiration_date": "20261231"}