Package 72189-586-30

Brand: quetiapine fumarate er

Generic: quetiapine fumarate er
NDC Package

Package Facts

Identity

Package NDC 72189-586-30
Digits Only 7218958630
Product NDC 72189-586
Product ID 72189-586_23820efc-4df8-9dc9-e063-6394a90a0bb4
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-586-30)

Marketing

Marketing Status
Marketed Since 2024-10-02
Brand quetiapine fumarate er
Generic quetiapine fumarate er
Sample Package No

Linked Drug Pages (1)

Quetiapine Fumarate ER ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "23820efc-4df8-9dc9-e063-6394a90a0bb4", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["895670"], "spl_set_id": ["23820efc-4df7-9dc9-e063-6394a90a0bb4"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-586-30)", "package_ndc": "72189-586-30", "marketing_start_date": "20241002"}], "brand_name": "Quetiapine Fumarate ER", "product_id": "72189-586_23820efc-4df8-9dc9-e063-6394a90a0bb4", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72189-586", "generic_name": "Quetiapine Fumarate ER", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine Fumarate ER", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "150 mg/1"}], "application_number": "ANDA209635", "marketing_category": "ANDA", "marketing_start_date": "20241002", "listing_expiration_date": "20261231"}