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United States · US · US:71335-0639_aa348cf2-2e1b-486f-9bec-5ccf67879175
LAMIVUDINE and ZIDOVUDINE
Orange BookUNIISPLATC J05AF
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeJ05AF
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1171335063916 TABLET, FILM COATED in 1 BOTTLE (71335-0639-1)
- ndc11713350639260 TABLET, FILM COATED in 1 BOTTLE (71335-0639-2)
- ndc1171335063934 TABLET, FILM COATED in 1 BOTTLE (71335-0639-3)
Annotations
UNII (FDA Substance ID)
2T8Q726O95
LAMIVUDINE
RxCUI 68244
Orange Book
A079124
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "2T8Q726O95",
"rxcui": "68244",
"inchikey": "JTEGQNOMFQHVDC-NKWVEPMBSA-N",
"display_name": "LAMIVUDINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"6fd4d6b9-65ea-4988-8d6f-dd220ec5052d": {
"match": "brand_token",
"title": "LAMIVUDINE TABLET, FILM COATED [MAJOR PHARMACEUTICALS]",
"spl_version": "5",
"published_date": "2026-03-20"
}
},
"productid": "71335-0639_aa348cf2-2e1b-486f-9bec-5ccf67879175",
"productndc": "71335-0639",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "079124",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "150MG;300MG",
"product_no": "001",
"approval_date": "Sep 17, 2015"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LAMIVUDINE; ZIDOVUDINE",
"proprietary_name": "LAMIVUDINE and ZIDOVUDINE",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "ANDA079124",
"marketing_category": "ANDA",
"nonproprietary_name": "LAMIVUDINE and ZIDOVUDINE",
"start_marketing_date": "20150918",
"active_numerator_strength": "150; 300"
}Related drugs
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- GBAbacavir 600mg / Lamivudine 300mg tabletsA A H Pharmaceuticals Ltd
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