Package 72789-266-07

Brand: quetiapine

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 72789-266-07
Digits Only 7278926607
Product NDC 72789-266
Product ID 72789-266_31b9bfe1-9c84-b590-e063-6294a90a482c
Description

7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-266-07)

Marketing

Marketing Status
Marketed Since 2022-08-16
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": "31b9bfe1-9c84-b590-e063-6294a90a482c", "openfda": {"upc": ["0372789266077"], "unii": ["2S3PL1B6UJ"], "rxcui": ["616487"], "spl_set_id": ["da3c9642-9f8d-422b-8e12-2036d68f78ca"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-266-07)", "package_ndc": "72789-266-07", "marketing_start_date": "20220816"}], "brand_name": "Quetiapine", "product_id": "72789-266_31b9bfe1-9c84-b590-e063-6294a90a482c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72789-266", "generic_name": "Quetiapine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "50 mg/1"}], "application_number": "ANDA201504", "marketing_category": "ANDA", "marketing_start_date": "20130301", "listing_expiration_date": "20261231"}