Package 68071-3931-9

Brand: quetiapine fumarate

Generic: quetiapine fumarate
NDC Package

Package Facts

Identity

Package NDC 68071-3931-9
Digits Only 6807139319
Product NDC 68071-3931
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3931-9)

Marketing

Marketing Status
Marketed Since 2025-12-09
Brand quetiapine fumarate
Generic quetiapine fumarate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "458cae68-c11e-e760-e063-6394a90ac04e", "openfda": {"upc": ["0368071393194"], "unii": ["2S3PL1B6UJ"], "rxcui": ["312744"], "spl_set_id": ["458cae68-c11d-e760-e063-6394a90ac04e"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3931-9)", "package_ndc": "68071-3931-9", "marketing_start_date": "20251209"}], "brand_name": "Quetiapine Fumarate", "product_id": "68071-3931_458cae68-c11e-e760-e063-6394a90ac04e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68071-3931", "generic_name": "Quetiapine Fumarate", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine Fumarate", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "25 mg/1"}], "application_number": "ANDA202674", "marketing_category": "ANDA", "marketing_start_date": "20160701", "listing_expiration_date": "20261231"}