Package 71093-135-02
Brand: quetiapine extended release
Generic: quetiapinePackage Facts
Identity
Package NDC
71093-135-02
Digits Only
7109313502
Product NDC
71093-135
Description
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71093-135-02)
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": "8a3515c7-6fc7-4150-a898-23443e4802fd", "openfda": {"upc": ["0371093135024", "0371093137028", "0371093136021", "0371093138025"], "unii": ["2S3PL1B6UJ"], "rxcui": ["721791", "721794", "721796", "853201", "895670"], "spl_set_id": ["07e4f3f4-42cb-4b22-bf8d-8c3279d26e97"], "manufacturer_name": ["ACI Healthcare USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71093-135-02)", "package_ndc": "71093-135-02", "marketing_start_date": "20190130"}], "brand_name": "Quetiapine Extended Release", "product_id": "71093-135_8a3515c7-6fc7-4150-a898-23443e4802fd", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "71093-135", "generic_name": "Quetiapine", "labeler_name": "ACI Healthcare USA, 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"}