Package 68180-615-07

Brand: quetiapine

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 68180-615-07
Digits Only 6818061507
Product NDC 68180-615
Product ID 68180-615_851955c8-57fc-490c-b7a8-15a6c87ff06e
Description

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-615-07)

Marketing

Marketing Status
Marketed Since 2017-08-22
Brand quetiapine
Generic quetiapine
Sample Package No

Linked Drug Pages (1)

Quetiapine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "851955c8-57fc-490c-b7a8-15a6c87ff06e", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["721791", "721794", "721796", "853201", "895670"], "spl_set_id": ["7803a290-91c0-4e7f-90b5-d2ff33a46cee"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-615-07)", "package_ndc": "68180-615-07", "marketing_start_date": "20170822"}], "brand_name": "Quetiapine", "product_id": "68180-615_851955c8-57fc-490c-b7a8-15a6c87ff06e", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68180-615", "generic_name": "Quetiapine", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "300 mg/1"}], "application_number": "ANDA204203", "marketing_category": "ANDA", "marketing_start_date": "20170822", "listing_expiration_date": "20261231"}