Package 67296-2138-2

Brand: meclizine hydrochloride

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67296-2138-2
Digits Only 6729621382
Product NDC 67296-2138
Product ID 67296-2138_46acae7b-a761-bb45-e063-6394a90af94c
Description

21 TABLET in 1 BOTTLE (67296-2138-2)

Marketing

Marketing Status
Marketed Since 2020-10-29
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": "46acae7b-a761-bb45-e063-6394a90af94c", "openfda": {"upc": ["0370710116118"], "unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["37457bd5-2fdd-b829-e063-6294a90a04f0"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE (67296-2138-2)", "package_ndc": "67296-2138-2", "marketing_start_date": "20201029"}], "brand_name": "Meclizine Hydrochloride", "product_id": "67296-2138_46acae7b-a761-bb45-e063-6394a90af94c", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "67296-2138", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA213957", "marketing_category": "ANDA", "marketing_start_date": "20201029", "listing_expiration_date": "20261231"}