Package 0093-2063-01

Brand: quetiapine

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 0093-2063-01
Digits Only 0093206301
Product NDC 0093-2063
Product ID 0093-2063_5059f747-d59d-460b-99bc-7b76b235c094
Description

100 TABLET, FILM COATED in 1 BOTTLE (0093-2063-01)

Marketing

Marketing Status
Marketed Since 2014-03-12
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": "5059f747-d59d-460b-99bc-7b76b235c094", "openfda": {"upc": ["0300938163014", "0300932063013", "0300938162017", "0300938164011", "0300938166015"], "unii": ["2S3PL1B6UJ"], "rxcui": ["312743", "312744", "312745", "317174", "616483", "616487"], "spl_set_id": ["c1d4ef59-bf58-44fe-9b46-1af42e2f7f8b"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-2063-01)", "package_ndc": "0093-2063-01", "marketing_start_date": "20140312"}], "brand_name": "Quetiapine", "product_id": "0093-2063_5059f747-d59d-460b-99bc-7b76b235c094", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0093-2063", "generic_name": "Quetiapine", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "25 mg/1"}], "application_number": "ANDA077745", "marketing_category": "ANDA", "marketing_start_date": "20140312", "listing_expiration_date": "20271231"}