Package 42708-127-30

Brand: meclizine hydrochloride

Generic: meclizine hydrochloride
NDC Package Sample

Package Facts

Identity

Package NDC 42708-127-30
Digits Only 4270812730
Product NDC 42708-127
Product ID 42708-127_459bfdd2-c97a-ba9e-e063-6394a90a5d43
Description

30 TABLET in 1 BOTTLE (42708-127-30)

Marketing

Marketing Status
Marketed Since 2018-05-23
Brand meclizine hydrochloride
Generic meclizine hydrochloride
Sample Package Yes

Linked Drug Pages (1)

Meclizine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "459bfdd2-c97a-ba9e-e063-6394a90a5d43", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["18fe5e13-5583-45ee-ab6e-32e9af426bd8"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE (42708-127-30)", "package_ndc": "42708-127-30", "marketing_start_date": "20180523"}], "brand_name": "Meclizine Hydrochloride", "product_id": "42708-127_459bfdd2-c97a-ba9e-e063-6394a90a5d43", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "42708-127", "generic_name": "Meclizine Hydrochloride", "labeler_name": "QPharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA201451", "marketing_category": "ANDA", "marketing_start_date": "20100212", "listing_expiration_date": "20261231"}