Package 71335-2641-1

Brand: quetiapine

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 71335-2641-1
Digits Only 7133526411
Product NDC 71335-2641
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2641-1)

Marketing

Marketing Status
Marketed Since 2025-06-02
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": "a6ac6b04-2df1-4c0b-9e26-1db660b84d15", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["721796"], "spl_set_id": ["a373a57d-1dee-4bd1-b71b-494e1662f558"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2641-1)", "package_ndc": "71335-2641-1", "marketing_start_date": "20250602"}], "brand_name": "Quetiapine", "product_id": "71335-2641_a6ac6b04-2df1-4c0b-9e26-1db660b84d15", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "71335-2641", "generic_name": "Quetiapine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "400 mg/1"}], "application_number": "ANDA215478", "marketing_category": "ANDA", "marketing_start_date": "20220815", "listing_expiration_date": "20261231"}