Package 71335-2176-2
Brand: quetiapine fumarate
Generic: quetiapine fumaratePackage Facts
Identity
Package NDC
71335-2176-2
Digits Only
7133521762
Product NDC
71335-2176
Description
60 TABLET, FILM COATED in 1 BOTTLE (71335-2176-2)
Marketing
Marketing Status
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": "35073226-49ae-4460-e063-6294a90a54cf", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["616487"], "spl_set_id": ["3eb39b4e-4c79-43b9-a30e-b4221c0e2bd2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2176-1)", "package_ndc": "71335-2176-1", "marketing_start_date": "20221010"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2176-2)", "package_ndc": "71335-2176-2", "marketing_start_date": "20221017"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2176-3)", "package_ndc": "71335-2176-3", "marketing_start_date": "20240403"}, {"sample": false, "description": "25 TABLET, FILM COATED in 1 BOTTLE (71335-2176-4)", "package_ndc": "71335-2176-4", "marketing_start_date": "20240403"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-2176-5)", "package_ndc": "71335-2176-5", "marketing_start_date": "20240403"}], "brand_name": "Quetiapine fumarate", "product_id": "71335-2176_35073226-49ae-4460-e063-6294a90a54cf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "71335-2176", "generic_name": "Quetiapine fumarate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine fumarate", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "50 mg/1"}], "application_number": "ANDA201190", "marketing_category": "ANDA", "marketing_start_date": "20120328", "listing_expiration_date": "20261231"}