Package 61269-255-10

Brand: seroquel

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 61269-255-10
Digits Only 6126925510
Product NDC 61269-255
Description

100 TABLET, FILM COATED in 1 BOTTLE (61269-255-10)

Marketing

Marketing Status
Marketed Since 2006-02-13
Brand seroquel
Generic quetiapine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c66b0a69-3827-4a3f-a506-55b674865b2b", "openfda": {"unii": ["2S3PL1B6UJ"], "spl_set_id": ["8ae62aaf-f8c5-417f-baac-0098369ca322"], "manufacturer_name": ["H2-Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (61269-255-10)", "package_ndc": "61269-255-10", "marketing_start_date": "20060213"}], "brand_name": "SEROQUEL", "product_id": "61269-255_c66b0a69-3827-4a3f-a506-55b674865b2b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "61269-255", "generic_name": "quetiapine", "labeler_name": "H2-Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SEROQUEL", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "400 mg/1"}], "application_number": "NDA020639", "marketing_category": "NDA", "marketing_start_date": "20060213", "listing_expiration_date": "20261231"}