Package 72189-237-90
Brand: meclizine hydrochloride
Generic: meclizine hydrochloridePackage Facts
Identity
Package NDC
72189-237-90
Digits Only
7218923790
Product NDC
72189-237
Description
90 TABLET in 1 BOTTLE (72189-237-90)
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": "15ac00f8-da4e-6cea-e063-6294a90aeb81", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["e79ecf77-0e0a-d7ef-e053-2a95a90a5adf"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-237-30)", "package_ndc": "72189-237-30", "marketing_start_date": "20220901"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-237-90)", "package_ndc": "72189-237-90", "marketing_start_date": "20220901"}], "brand_name": "Meclizine Hydrochloride", "product_id": "72189-237_15ac00f8-da4e-6cea-e063-6294a90aeb81", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "72189-237", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Direct_Rx", "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": "20220901", "listing_expiration_date": "20261231"}