Package 60760-866-30

Brand: quetiapine extended release

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 60760-866-30
Digits Only 6076086630
Product NDC 60760-866
Product ID 60760-866_3622ca24-c93a-c2af-e063-6394a90a1a41
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-866-30)

Marketing

Marketing Status
Marketed Since 2025-05-19
Brand quetiapine extended release
Generic quetiapine
Sample Package No

Linked Drug Pages (1)

Quetiapine Extended Release ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3622ca24-c93a-c2af-e063-6394a90a1a41", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["721791"], "spl_set_id": ["3622cbd4-d7cb-57d4-e063-6294a90a5f24"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-866-30)", "package_ndc": "60760-866-30", "marketing_start_date": "20250519"}], "brand_name": "Quetiapine Extended Release", "product_id": "60760-866_3622ca24-c93a-c2af-e063-6394a90a1a41", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "60760-866", "generic_name": "Quetiapine", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "brand_name_suffix": "Extended Release", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "200 mg/1"}], "application_number": "ANDA209635", "marketing_category": "ANDA", "marketing_start_date": "20171129", "listing_expiration_date": "20261231"}