Package 61269-270-60

Brand: seroquel xr

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 61269-270-60
Digits Only 6126927060
Product NDC 61269-270
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (61269-270-60)

Marketing

Marketing Status
Marketed Since 2009-02-01
Brand seroquel xr
Generic quetiapine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "429359fa-9bf0-42d7-af7b-6b153d1c03b8", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["721791", "721793", "721794", "721795", "721796", "721797", "853201", "853202", "895670", "895671"], "spl_set_id": ["ab959a35-d0ba-4f18-8f2e-6619d88b16e3"], "manufacturer_name": ["H2-Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (61269-270-60)", "package_ndc": "61269-270-60", "marketing_start_date": "20090201"}], "brand_name": "SEROQUEL XR", "product_id": "61269-270_429359fa-9bf0-42d7-af7b-6b153d1c03b8", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "61269-270", "generic_name": "quetiapine", "labeler_name": "H2-Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SEROQUEL", "brand_name_suffix": "XR", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "50 mg/1"}], "application_number": "NDA022047", "marketing_category": "NDA", "marketing_start_date": "20090201", "listing_expiration_date": "20261231"}