Package 49884-720-08

Brand: sapropterin dihydrochloride

Generic: sapropterin dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 49884-720-08
Digits Only 4988472008
Product NDC 49884-720
Description

120 TABLET in 1 BOTTLE (49884-720-08)

Marketing

Marketing Status
Marketed Since 2020-10-01
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": "19c41225-2753-4069-9a72-7bcd9590f96c", "openfda": {"upc": ["0349884720087"], "unii": ["RG277LF5B3"], "rxcui": ["1486687"], "spl_set_id": ["eafec3a2-4f29-4afa-8728-a62b34cefd18"], "manufacturer_name": ["ENDO USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (49884-720-08)", "package_ndc": "49884-720-08", "marketing_start_date": "20201001"}], "brand_name": "sapropterin dihydrochloride", "product_id": "49884-720_19c41225-2753-4069-9a72-7bcd9590f96c", "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": "49884-720", "generic_name": "sapropterin dihydrochloride", "labeler_name": "ENDO USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "sapropterin dihydrochloride", "active_ingredients": [{"name": "SAPROPTERIN DIHYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA207200", "marketing_category": "ANDA", "marketing_start_date": "20201001", "listing_expiration_date": "20261231"}