Package 80425-0494-1
Brand: meclizine hydrochloride
Generic: meclizine hydrochloridePackage Facts
Identity
Package NDC
80425-0494-1
Digits Only
8042504941
Product NDC
80425-0494
Description
30 TABLET in 1 BOTTLE (80425-0494-1)
Marketing
Marketing Status
Brand
meclizine hydrochloride
Generic
meclizine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d31baa5-5e96-61fa-e063-6394a90a7413", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["2d31ae73-3f09-a77c-e063-6294a90ade9a"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0494-1)", "package_ndc": "80425-0494-1", "marketing_start_date": "20250202"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0494-2)", "package_ndc": "80425-0494-2", "marketing_start_date": "20250202"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (80425-0494-3)", "package_ndc": "80425-0494-3", "marketing_start_date": "20250202"}], "brand_name": "Meclizine Hydrochloride", "product_id": "80425-0494_2d31baa5-5e96-61fa-e063-6394a90a7413", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "80425-0494", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "NDA010721", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20250202", "listing_expiration_date": "20261231"}