Package 65862-877-01
Brand: quetiapine fumarate
Generic: quetiapinePackage Facts
Identity
Package NDC
65862-877-01
Digits Only
6586287701
Product NDC
65862-877
Description
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-877-01)
Marketing
Marketing Status
Brand
quetiapine fumarate
Generic
quetiapine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "631d518f-bb71-4848-98a6-f9335dc5b33b", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["721791", "721794", "721796", "853201", "895670"], "spl_set_id": ["6562eb60-0d70-4909-bd07-88d5c9241516"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-877-01)", "package_ndc": "65862-877-01", "marketing_start_date": "20171129"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-877-05)", "package_ndc": "65862-877-05", "marketing_start_date": "20171129"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-877-60)", "package_ndc": "65862-877-60", "marketing_start_date": "20171129"}], "brand_name": "Quetiapine Fumarate", "product_id": "65862-877_631d518f-bb71-4848-98a6-f9335dc5b33b", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "65862-877", "generic_name": "Quetiapine", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine Fumarate", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "400 mg/1"}], "application_number": "ANDA207655", "marketing_category": "ANDA", "marketing_start_date": "20171129", "listing_expiration_date": "20261231"}