Package 68071-3921-6
Brand: quetiapine extended release
Generic: quetiapinePackage Facts
Identity
Package NDC
68071-3921-6
Digits Only
6807139216
Product NDC
68071-3921
Description
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-3921-6)
Marketing
Marketing Status
Brand
quetiapine extended release
Generic
quetiapine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "44e9af46-3b06-d8ac-e063-6394a90a6bbb", "openfda": {"upc": ["0368071392166"], "unii": ["2S3PL1B6UJ"], "rxcui": ["853201"], "spl_set_id": ["44e9b338-b163-bee7-e063-6394a90a1338"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-3921-6)", "package_ndc": "68071-3921-6", "marketing_start_date": "20251201"}], "brand_name": "Quetiapine Extended Release", "product_id": "68071-3921_44e9af46-3b06-d8ac-e063-6394a90a6bbb", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68071-3921", "generic_name": "Quetiapine", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "brand_name_suffix": "Extended Release", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "50 mg/1"}], "application_number": "ANDA209635", "marketing_category": "ANDA", "marketing_start_date": "20171129", "listing_expiration_date": "20261231"}