Package 68001-599-06

Brand: quetiapine

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 68001-599-06
Digits Only 6800159906
Product NDC 68001-599
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-599-06)

Marketing

Marketing Status
Marketed Since 2023-11-28
Brand quetiapine
Generic quetiapine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "487e93eb-c251-17da-e063-6294a90a6517", "openfda": {"upc": ["0368001602068", "0368001599061", "0368001600064", "0368001601061", "0368001598064"], "unii": ["2S3PL1B6UJ"], "rxcui": ["721791", "721794", "721796", "853201", "895670"], "spl_set_id": ["186c5cde-5066-4436-99ef-28049c12826b"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-599-06)", "package_ndc": "68001-599-06", "marketing_start_date": "20231128"}], "brand_name": "Quetiapine", "product_id": "68001-599_487e93eb-c251-17da-e063-6294a90a6517", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68001-599", "generic_name": "Quetiapine", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "150 mg/1"}], "application_number": "ANDA215478", "marketing_category": "ANDA", "marketing_start_date": "20231101", "listing_expiration_date": "20271231"}