Package 72189-302-30

Brand: meclizine hydrochloride

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72189-302-30
Digits Only 7218930230
Product NDC 72189-302
Product ID 72189-302_2c2959f7-0f30-7cda-e063-6294a90a2b82
Description

30 TABLET in 1 BOTTLE (72189-302-30)

Marketing

Marketing Status
Marketed Since 2021-12-06
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": "2c2959f7-0f30-7cda-e063-6294a90a2b82", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624"], "spl_set_id": ["d27fe828-4fee-3ba9-e053-2995a90ae7b6"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-302-30)", "package_ndc": "72189-302-30", "marketing_start_date": "20211206"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-302-60)", "package_ndc": "72189-302-60", "marketing_start_date": "20211206"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "72189-302_2c2959f7-0f30-7cda-e063-6294a90a2b82", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "72189-302", "generic_name": "MECLIZINE HYDROCHLORIDE", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MECLIZINE HYDROCHLORIDE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "NDA010721", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20211206", "listing_expiration_date": "20261231"}