Package 72189-519-30

Brand: quetiapine fumarate er

Generic: quetiapine fumarate er
NDC Package

Package Facts

Identity

Package NDC 72189-519-30
Digits Only 7218951930
Product NDC 72189-519
Product ID 72189-519_2c4e7611-7a3a-f31d-e063-6394a90a236f
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-519-30)

Marketing

Marketing Status
Marketed Since 2023-11-01
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": "2c4e7611-7a3a-f31d-e063-6394a90a236f", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["721791"], "spl_set_id": ["0917ef53-2647-b54b-e063-6294a90a4211"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-519-30)", "package_ndc": "72189-519-30", "marketing_start_date": "20231101"}], "brand_name": "Quetiapine Fumarate ER", "product_id": "72189-519_2c4e7611-7a3a-f31d-e063-6394a90a236f", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72189-519", "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": "200 mg/1"}], "application_number": "ANDA209635", "marketing_category": "ANDA", "marketing_start_date": "20231101", "listing_expiration_date": "20261231"}