Package 79739-7143-1

Brand: ursodiol 200 mg

Generic: usodiol
NDC Package

Package Facts

Identity

Package NDC 79739-7143-1
Digits Only 7973971431
Product NDC 79739-7143
Description

100 CAPSULE in 1 BOTTLE (79739-7143-1)

Marketing

Marketing Status
Marketed Since 2020-07-01
Brand ursodiol 200 mg
Generic usodiol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "efdeb26d-50b6-4a2f-886a-fcb59ea7fee0", "openfda": {"nui": ["N0000175802", "M0002475"], "unii": ["724L30Y2QR"], "rxcui": ["412174", "2376942"], "spl_set_id": ["ebaaa3e2-1d80-4b40-b696-88cdd06448e4"], "pharm_class_cs": ["Bile Acids and Salts [CS]"], "pharm_class_epc": ["Bile Acid [EPC]"], "manufacturer_name": ["LGM PHARMA SOLUTIONS, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (79739-7143-1)", "package_ndc": "79739-7143-1", "marketing_start_date": "20200701"}], "brand_name": "Ursodiol 200 mg", "product_id": "79739-7143_efdeb26d-50b6-4a2f-886a-fcb59ea7fee0", "dosage_form": "CAPSULE", "pharm_class": ["Bile Acid [EPC]", "Bile Acids and Salts [CS]"], "product_ndc": "79739-7143", "generic_name": "Usodiol", "labeler_name": "LGM PHARMA SOLUTIONS, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ursodiol 200 mg", "active_ingredients": [{"name": "URSODIOL", "strength": "200 mg/1"}], "application_number": "ANDA205789", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}