Package 76282-677-30

Brand: emtricitabine and tenofovir disoproxil fumarate

Generic: emtricitabine and tenofovir disoproxil fumarate
NDC Package

Package Facts

Identity

Package NDC 76282-677-30
Digits Only 7628267730
Product NDC 76282-677
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76282-677-30)

Marketing

Marketing Status
Marketed Since 2021-04-06
Brand emtricitabine and tenofovir disoproxil fumarate
Generic emtricitabine and tenofovir disoproxil fumarate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09bb7f3f-5d80-4f4b-b681-4878830cd971", "openfda": {"nui": ["N0000175462", "M0015066", "N0000009947"], "unii": ["G70B4ETF4S", "OTT9J7900I"], "rxcui": ["476556"], "spl_set_id": ["31af598d-6ef2-469b-ac4c-3ac805e6fa44"], "pharm_class_cs": ["Nucleosides [CS]"], "pharm_class_epc": ["Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]"], "pharm_class_moa": ["Nucleoside Reverse Transcriptase Inhibitors [MoA]"], "manufacturer_name": ["Exelan Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76282-677-30)", "package_ndc": "76282-677-30", "marketing_start_date": "20210406"}], "brand_name": "EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE", "product_id": "76282-677_09bb7f3f-5d80-4f4b-b681-4878830cd971", "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]", "Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]", "Nucleoside Reverse Transcriptase Inhibitors [MoA]", "Nucleoside Reverse Transcriptase Inhibitors [MoA]", "Nucleosides [CS]", "Nucleosides [CS]"], "product_ndc": "76282-677", "generic_name": "EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE", "labeler_name": "Exelan Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE", "active_ingredients": [{"name": "EMTRICITABINE", "strength": "200 mg/1"}, {"name": "TENOFOVIR DISOPROXIL FUMARATE", "strength": "300 mg/1"}], "application_number": "ANDA090958", "marketing_category": "ANDA", "marketing_start_date": "20210406", "listing_expiration_date": "20261231"}