Package 72603-191-01
Brand: sapropterin dihydrochloride
Generic: sapropterin dihydrochloridePackage Facts
Identity
Package NDC
72603-191-01
Digits Only
7260319101
Product NDC
72603-191
Description
120 TABLET in 1 BOTTLE (72603-191-01)
Marketing
Marketing Status
Brand
sapropterin dihydrochloride
Generic
sapropterin dihydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b08d642-3262-b372-e063-6294a90afc2a", "openfda": {"upc": ["0372603191011"], "unii": ["RG277LF5B3"], "rxcui": ["1486687"], "spl_set_id": ["a64a50ba-e3da-4227-9bce-87101d60409e"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (72603-191-01)", "package_ndc": "72603-191-01", "marketing_start_date": "20231201"}], "brand_name": "sapropterin dihydrochloride", "product_id": "72603-191_2b08d642-3262-b372-e063-6294a90afc2a", "dosage_form": "TABLET", "pharm_class": ["Breast Cancer Resistance Protein Inhibitors [MoA]", "P-Glycoprotein Inhibitors [MoA]", "Phenylalanine Hydroxylase Activator [EPC]", "Phenylalanine Hydroxylase Activators [MoA]"], "product_ndc": "72603-191", "generic_name": "sapropterin dihydrochloride", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "sapropterin dihydrochloride", "active_ingredients": [{"name": "SAPROPTERIN DIHYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA215534", "marketing_category": "ANDA", "marketing_start_date": "20231201", "listing_expiration_date": "20261231"}