Package 68071-1669-6

Brand: quetiapine fumarate

Generic: quetiapine fumarate
NDC Package

Package Facts

Identity

Package NDC 68071-1669-6
Digits Only 6807116696
Product NDC 68071-1669
Description

60 TABLET, FILM COATED in 1 BOTTLE (68071-1669-6)

Marketing

Marketing Status
Marketed Since 2024-01-23
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": "0fdc0739-3333-c566-e063-6294a90a7740", "openfda": {"upc": ["0368071166965"], "unii": ["2S3PL1B6UJ"], "rxcui": ["312745"], "spl_set_id": ["0fdbe32f-d04a-5666-e063-6294a90a8e36"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68071-1669-6)", "package_ndc": "68071-1669-6", "marketing_start_date": "20240123"}], "brand_name": "Quetiapine Fumarate", "product_id": "68071-1669_0fdc0739-3333-c566-e063-6294a90a7740", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68071-1669", "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": "300 mg/1"}], "application_number": "ANDA091388", "marketing_category": "ANDA", "marketing_start_date": "20120327", "listing_expiration_date": "20261231"}