Package 75987-060-08

Brand: buphenyl

Generic: sodium phenylbutyrate
NDC Package

Package Facts

Identity

Package NDC 75987-060-08
Digits Only 7598706008
Product NDC 75987-060
Product ID 75987-060_3178e0bc-ebb7-4ddd-be43-630ff87eeb02
Description

1 BOTTLE in 1 CARTON (75987-060-08) / 250 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 1996-05-13
Brand buphenyl
Generic sodium phenylbutyrate
Sample Package No

Linked Drug Pages (1)

BUPHENYL, Buphenyl ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3178e0bc-ebb7-4ddd-be43-630ff87eeb02", "openfda": {"unii": ["NT6K61736T"], "rxcui": ["199369", "213196", "984105", "984107"], "spl_set_id": ["463a36fa-3eb2-4326-8bd0-c8c7a11bca3a"], "manufacturer_name": ["Horizon Therapeutics USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (75987-060-08)  / 250 TABLET in 1 BOTTLE", "package_ndc": "75987-060-08", "marketing_start_date": "19960513"}], "brand_name": "BUPHENYL", "product_id": "75987-060_3178e0bc-ebb7-4ddd-be43-630ff87eeb02", "dosage_form": "TABLET", "pharm_class": ["Ammonium Ion Binding Activity [MoA]", "Nitrogen Binding Agent [EPC]"], "product_ndc": "75987-060", "generic_name": "sodium phenylbutyrate", "labeler_name": "Horizon Therapeutics USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUPHENYL", "active_ingredients": [{"name": "SODIUM PHENYLBUTYRATE", "strength": "500 mg/1"}], "application_number": "NDA020572", "marketing_category": "NDA", "marketing_start_date": "19960513", "listing_expiration_date": "20261231"}