Package 67296-2205-3

Brand: meclizine hydrochloride

Generic: meclizine
NDC Package

Package Facts

Identity

Package NDC 67296-2205-3
Digits Only 6729622053
Product NDC 67296-2205
Product ID 67296-2205_4727eeb1-e0a4-a92c-e063-6394a90af806
Description

30 TABLET in 1 BOTTLE (67296-2205-3)

Marketing

Marketing Status
Marketed Since 2023-09-14
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": "4727eeb1-e0a4-a92c-e063-6394a90af806", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["4727e7a9-eabb-a2a7-e063-6394a90a8754"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-2205-3)", "package_ndc": "67296-2205-3", "marketing_start_date": "20230914"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "67296-2205_4727eeb1-e0a4-a92c-e063-6394a90af806", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "67296-2205", "generic_name": "MECLIZINE", "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": "ANDA202640", "marketing_category": "ANDA", "marketing_start_date": "20230914", "listing_expiration_date": "20261231"}