Package 72189-366-30

Brand: quetiapine fumarate

Generic: quetiapine fumarate
NDC Package

Package Facts

Identity

Package NDC 72189-366-30
Digits Only 7218936630
Product NDC 72189-366
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-366-30)

Marketing

Marketing Status
Marketed Since 2022-07-27
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": "37b38291-50c8-00c9-e063-6394a90a83ef", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["616487"], "spl_set_id": ["e4ce9d50-9786-2233-e053-2a95a90a276f"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-366-30)", "package_ndc": "72189-366-30", "marketing_start_date": "20220727"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72189-366-60)", "package_ndc": "72189-366-60", "marketing_start_date": "20220727"}], "brand_name": "Quetiapine Fumarate", "product_id": "72189-366_37b38291-50c8-00c9-e063-6394a90a83ef", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72189-366", "generic_name": "Quetiapine Fumarate", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine Fumarate", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "50 mg/1"}], "application_number": "ANDA201504", "marketing_category": "ANDA", "marketing_start_date": "20220727", "listing_expiration_date": "20261231"}