Package 0904-6890-04

Brand: ursodiol

Generic: ursodiol
NDC Package

Package Facts

Identity

Package NDC 0904-6890-04
Digits Only 0904689004
Product NDC 0904-6890
Product ID 0904-6890_ca0b53eb-7518-475a-9b3e-0dec31111904
Description

30 BLISTER PACK in 1 CARTON (0904-6890-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2013-08-01
Brand ursodiol
Generic ursodiol
Sample Package No

Linked Drug Pages (1)

Ursodiol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ca0b53eb-7518-475a-9b3e-0dec31111904", "openfda": {"nui": ["N0000175802", "M0002475"], "unii": ["724L30Y2QR"], "rxcui": ["858751"], "spl_set_id": ["e1f6abfd-2158-4824-b53d-717fbe6de3f9"], "pharm_class_cs": ["Bile Acids and Salts [CS]"], "pharm_class_epc": ["Bile Acid [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-6890-04)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6890-04", "marketing_start_date": "20130801"}], "brand_name": "Ursodiol", "product_id": "0904-6890_ca0b53eb-7518-475a-9b3e-0dec31111904", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bile Acid [EPC]", "Bile Acids and Salts [CS]"], "product_ndc": "0904-6890", "generic_name": "Ursodiol", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ursodiol", "active_ingredients": [{"name": "URSODIOL", "strength": "250 mg/1"}], "application_number": "ANDA202540", "marketing_category": "ANDA", "marketing_start_date": "20130801", "listing_expiration_date": "20261231"}