Package 33342-135-09

Brand: quetiapine

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 33342-135-09
Digits Only 3334213509
Product NDC 33342-135
Product ID 33342-135_fb91b782-1195-4212-b130-9e078dc47dcd
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-135-09)

Marketing

Marketing Status
Marketed Since 2017-11-01
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": "fb91b782-1195-4212-b130-9e078dc47dcd", "openfda": {"upc": ["0333342134158", "0333342137098", "0333342136091", "0333342135094", "0333342136152", "0333342137159", "0333342134097"], "unii": ["2S3PL1B6UJ"], "rxcui": ["721791", "721794", "721796", "895670"], "spl_set_id": ["d699b8c7-8a1c-44ed-85d8-c821a9c8c848"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-135-09)", "package_ndc": "33342-135-09", "marketing_start_date": "20171101"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-135-15)", "package_ndc": "33342-135-15", "marketing_start_date": "20171101"}], "brand_name": "QUETIAPINE", "product_id": "33342-135_fb91b782-1195-4212-b130-9e078dc47dcd", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "33342-135", "generic_name": "QUETIAPINE", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "QUETIAPINE", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "200 mg/1"}], "application_number": "ANDA204253", "marketing_category": "ANDA", "marketing_start_date": "20171101", "listing_expiration_date": "20261231"}