Package 49884-413-01

Brand: ursodiol

Generic: ursodiol
NDC Package

Package Facts

Identity

Package NDC 49884-413-01
Digits Only 4988441301
Product NDC 49884-413
Product ID 49884-413_e0a305a9-0627-494f-aa1d-117c45eba561
Description

100 TABLET, FILM COATED in 1 BOTTLE (49884-413-01)

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": "e0a305a9-0627-494f-aa1d-117c45eba561", "openfda": {"nui": ["N0000175802", "M0002475"], "upc": ["0349884412012", "0349884413019"], "unii": ["724L30Y2QR"], "rxcui": ["858733", "858751"], "spl_set_id": ["1a3a8942-94d4-4292-bf74-0a67d92acb90"], "pharm_class_cs": ["Bile Acids and Salts [CS]"], "pharm_class_epc": ["Bile Acid [EPC]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (49884-413-01)", "package_ndc": "49884-413-01", "marketing_start_date": "20130801"}], "brand_name": "Ursodiol", "product_id": "49884-413_e0a305a9-0627-494f-aa1d-117c45eba561", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bile Acid [EPC]", "Bile Acids and Salts [CS]"], "product_ndc": "49884-413", "generic_name": "Ursodiol", "labeler_name": "Endo USA, Inc.", "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"}