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United States · US · US:71335-1916_ae1913db-ec19-4f19-9ca8-0c524410de4c
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
- ndc1171335191616 TABLET in 1 BOTTLE (71335-1916-1)
- ndc11713351916260 TABLET in 1 BOTTLE (71335-1916-2)
- ndc1171335191634 TABLET in 1 BOTTLE (71335-1916-3)
Annotations
UNII (FDA Substance ID)
2T8Q726O95
LAMIVUDINE
RxCUI 68244
Orange Book
A090679
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": "71335-1916_ae1913db-ec19-4f19-9ca8-0c524410de4c",
"productndc": "71335-1916",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "090679",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "150MG;300MG",
"product_no": "001",
"approval_date": "Aug 29, 2018"
}
],
"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": "ANDA090679",
"marketing_category": "ANDA",
"nonproprietary_name": "Lamivudine and Zidovudine",
"start_marketing_date": "20180830",
"active_numerator_strength": "150; 300"
}Related drugs
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