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United States · US · US:71335-2083_99e2c90f-c40d-47cd-aa57-b0d0aca07bda
Losartan Potassium
Orange BookUNIISPLATC C09CA01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeC09CA01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 8
- ndc11713352083130 TABLET, FILM COATED in 1 BOTTLE (71335-2083-1)
- ndc11713352083260 TABLET, FILM COATED in 1 BOTTLE (71335-2083-2)
- ndc11713352083390 TABLET, FILM COATED in 1 BOTTLE (71335-2083-3)
- ndc117133520834120 TABLET, FILM COATED in 1 BOTTLE (71335-2083-4)
- ndc117133520835100 TABLET, FILM COATED in 1 BOTTLE (71335-2083-5)
- ndc11713352083628 TABLET, FILM COATED in 1 BOTTLE (71335-2083-6)
- ndc11713352083710 TABLET, FILM COATED in 1 BOTTLE (71335-2083-7)
- ndc117133520838180 TABLET, FILM COATED in 1 BOTTLE (71335-2083-8)
Annotations
UNII (FDA Substance ID)
3ST302B24A
LOSARTAN POTASSIUM
RxCUI 203160
Orange Book
A091497
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "3ST302B24A",
"rxcui": "203160",
"inchikey": "OXCMYAYHXIHQOA-UHFFFAOYSA-N",
"display_name": "LOSARTAN POTASSIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"5f7612dc-dccf-49e2-b541-3dab9dc1f97a": {
"match": "brand_token",
"title": "LOSARTAN POTASSIUM TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]",
"spl_version": "30",
"published_date": "2026-06-01"
}
},
"productid": "71335-2083_99e2c90f-c40d-47cd-aa57-b0d0aca07bda",
"productndc": "71335-2083",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "091497",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "25MG",
"product_no": "001",
"approval_date": "Jun 6, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "50MG",
"product_no": "002",
"approval_date": "Jun 6, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "100MG",
"product_no": "003",
"approval_date": "Jun 6, 2011"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LOSARTAN POTASSIUM",
"proprietary_name": "Losartan Potassium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA091497",
"marketing_category": "ANDA",
"nonproprietary_name": "Losartan Potassium",
"start_marketing_date": "20140730",
"active_numerator_strength": "100"
}Related drugs
Other records sharing ATC code C09CA01.
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