Package 50090-7202-0
Brand: tenofovir disoproxil fumarate
Generic: tenofovir disoproxil fumaratePackage Facts
Identity
Package NDC
50090-7202-0
Digits Only
5009072020
Product NDC
50090-7202
Description
30 TABLET, FILM COATED in 1 BOTTLE (50090-7202-0)
Marketing
Marketing Status
Brand
tenofovir disoproxil fumarate
Generic
tenofovir disoproxil fumarate
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40466844-1948-49fd-abef-f4d0629c07bd", "openfda": {"unii": ["OTT9J7900I"], "rxcui": ["349251"], "spl_set_id": ["67e0e1b7-6a45-4d63-b569-00826832c25a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7202-0)", "package_ndc": "50090-7202-0", "marketing_start_date": "20240801"}], "brand_name": "Tenofovir Disoproxil Fumarate", "product_id": "50090-7202_40466844-1948-49fd-abef-f4d0629c07bd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]", "Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]", "Nucleoside Reverse Transcriptase Inhibitors [MoA]", "Nucleosides [CS]"], "product_ndc": "50090-7202", "generic_name": "Tenofovir Disoproxil Fumarate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tenofovir Disoproxil Fumarate", "active_ingredients": [{"name": "TENOFOVIR DISOPROXIL FUMARATE", "strength": "300 mg/1"}], "application_number": "ANDA090636", "marketing_category": "ANDA", "marketing_start_date": "20181112", "listing_expiration_date": "20261231"}