Package 72189-481-30

Brand: quetiapine fumarate er

Generic: quetiapine fumarate er
NDC Package

Package Facts

Identity

Package NDC 72189-481-30
Digits Only 7218948130
Product NDC 72189-481
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-481-30)

Marketing

Marketing Status
Marketed Since 2023-06-01
Brand quetiapine fumarate er
Generic quetiapine fumarate er
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4e167d-290b-0703-e063-6394a90a9132", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["895670"], "spl_set_id": ["fd11db2d-364d-9bd6-e053-6394a90ade0b"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-481-30)", "package_ndc": "72189-481-30", "marketing_start_date": "20230601"}], "brand_name": "Quetiapine Fumarate ER", "product_id": "72189-481_2c4e167d-290b-0703-e063-6394a90a9132", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72189-481", "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": "ANDA090681", "marketing_category": "ANDA", "marketing_start_date": "20230601", "listing_expiration_date": "20261231"}