Package 72189-465-30

Brand: quetiapine fumarate

Generic: quetiapine fumarate
NDC Package

Package Facts

Identity

Package NDC 72189-465-30
Digits Only 7218946530
Product NDC 72189-465
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-465-30)

Marketing

Marketing Status
Marketed Since 2023-05-03
Brand quetiapine fumarate
Generic quetiapine fumarate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4ded5c-1186-6387-e063-6294a90a6ab9", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["317174"], "spl_set_id": ["face6c19-3dd9-b188-e053-6294a90a62d0"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-465-30)", "package_ndc": "72189-465-30", "marketing_start_date": "20230503"}], "brand_name": "Quetiapine Fumarate", "product_id": "72189-465_2c4ded5c-1186-6387-e063-6294a90a6ab9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72189-465", "generic_name": "Quetiapine Fumarate", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine Fumarate", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "200 mg/1"}], "application_number": "ANDA091388", "marketing_category": "ANDA", "marketing_start_date": "20230503", "listing_expiration_date": "20261231"}