Package 72162-1501-1

Brand: ursodiol

Generic: ursodiol
NDC Package

Package Facts

Identity

Package NDC 72162-1501-1
Digits Only 7216215011
Product NDC 72162-1501
Description

100 TABLET, FILM COATED in 1 BOTTLE (72162-1501-1)

Marketing

Marketing Status
Marketed Since 2023-03-30
Brand ursodiol
Generic ursodiol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ef4f0687-2fd1-43b2-9c55-e678cadb53d1", "openfda": {"nui": ["N0000175802", "M0002475"], "unii": ["724L30Y2QR"], "rxcui": ["858733"], "spl_set_id": ["be811c61-5f48-4b03-94b6-e6941b595621"], "pharm_class_cs": ["Bile Acids and Salts [CS]"], "pharm_class_epc": ["Bile Acid [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-1501-1)", "package_ndc": "72162-1501-1", "marketing_start_date": "20230330"}], "brand_name": "Ursodiol", "product_id": "72162-1501_ef4f0687-2fd1-43b2-9c55-e678cadb53d1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bile Acid [EPC]", "Bile Acids and Salts [CS]"], "product_ndc": "72162-1501", "generic_name": "Ursodiol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ursodiol", "active_ingredients": [{"name": "URSODIOL", "strength": "500 mg/1"}], "application_number": "ANDA202540", "marketing_category": "ANDA", "marketing_start_date": "20130801", "listing_expiration_date": "20261231"}