Package 31722-752-31

Brand: lamivudine

Generic: lamivudine
NDC Package

Package Facts

Identity

Package NDC 31722-752-31
Digits Only 3172275231
Product NDC 31722-752
Description

10 TABLET, FILM COATED in 1 BLISTER PACK (31722-752-31)

Marketing

Marketing Status
Marketed Since 2014-01-02
Brand lamivudine
Generic lamivudine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b44d27b-b610-8078-e063-6394a90a72dd", "openfda": {"nui": ["N0000175656", "N0000175462", "N0000009947"], "upc": ["0331722752060", "0331722752602"], "unii": ["2T8Q726O95"], "rxcui": ["205328"], "spl_set_id": ["6bd6b9da-df69-46db-813e-4e7f3bdecf95"], "pharm_class_epc": ["Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]", "Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]"], "pharm_class_moa": ["Nucleoside Reverse Transcriptase Inhibitors [MoA]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "600 TABLET, FILM COATED in 1 BOTTLE (31722-752-06)", "package_ndc": "31722-752-06", "marketing_start_date": "20140102"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BLISTER PACK (31722-752-31)", "package_ndc": "31722-752-31", "marketing_start_date": "20140102"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 CARTON (31722-752-32)", "package_ndc": "31722-752-32", "marketing_start_date": "20140102"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (31722-752-60)", "package_ndc": "31722-752-60", "marketing_start_date": "20140102"}], "brand_name": "Lamivudine", "product_id": "31722-752_2b44d27b-b610-8078-e063-6394a90a72dd", "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]"], "product_ndc": "31722-752", "generic_name": "Lamivudine", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamivudine", "active_ingredients": [{"name": "LAMIVUDINE", "strength": "100 mg/1"}], "application_number": "ANDA203260", "marketing_category": "ANDA", "marketing_start_date": "20140102", "listing_expiration_date": "20261231"}