Package 72789-361-07

Brand: tenofovir disoproxil fumarate

Generic: tenofovir disoproxil fumarate
NDC Package

Package Facts

Identity

Package NDC 72789-361-07
Digits Only 7278936107
Product NDC 72789-361
Description

7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-361-07)

Marketing

Marketing Status
Marketed Since 2023-10-26
Brand tenofovir disoproxil fumarate
Generic tenofovir disoproxil fumarate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40bb71ff-3881-bd53-e063-6394a90a38ef", "openfda": {"upc": ["0372789361079"], "unii": ["OTT9J7900I"], "rxcui": ["349251"], "spl_set_id": ["08a30772-02fc-4f63-e063-6394a90afd43"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-361-07)", "package_ndc": "72789-361-07", "marketing_start_date": "20231026"}], "brand_name": "Tenofovir Disoproxil Fumarate", "product_id": "72789-361_40bb71ff-3881-bd53-e063-6394a90a38ef", "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": "72789-361", "generic_name": "Tenofovir Disoproxil Fumarate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20231026", "listing_expiration_date": "20261231"}