Package 71335-0639-1
Brand: lamivudine and zidovudine
Generic: lamivudine and zidovudinePackage Facts
Identity
Package NDC
71335-0639-1
Digits Only
7133506391
Product NDC
71335-0639
Description
6 TABLET, FILM COATED in 1 BOTTLE (71335-0639-1)
Marketing
Marketing Status
Brand
lamivudine and zidovudine
Generic
lamivudine and zidovudine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aa348cf2-2e1b-486f-9bec-5ccf67879175", "openfda": {"nui": ["N0000175656", "N0000175462", "N0000009947"], "unii": ["2T8Q726O95", "4B9XT59T7S"], "rxcui": ["200082"], "spl_set_id": ["005f1b9d-1950-4ef3-a9d6-c428a40a3630"], "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": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (71335-0639-1)", "package_ndc": "71335-0639-1", "marketing_start_date": "20210402"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0639-2)", "package_ndc": "71335-0639-2", "marketing_start_date": "20211227"}, {"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (71335-0639-3)", "package_ndc": "71335-0639-3", "marketing_start_date": "20211227"}], "brand_name": "LAMIVUDINE and ZIDOVUDINE", "product_id": "71335-0639_aa348cf2-2e1b-486f-9bec-5ccf67879175", "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]"], "product_ndc": "71335-0639", "generic_name": "LAMIVUDINE and ZIDOVUDINE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LAMIVUDINE and ZIDOVUDINE", "active_ingredients": [{"name": "LAMIVUDINE", "strength": "150 mg/1"}, {"name": "ZIDOVUDINE", "strength": "300 mg/1"}], "application_number": "ANDA079124", "marketing_category": "ANDA", "marketing_start_date": "20150918", "listing_expiration_date": "20261231"}