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United States · US · US:71335-1102_ee7edcfc-8787-49ba-810c-6c4f5d5fa8df
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
- ndc11713351102130 TABLET, FILM COATED in 1 BOTTLE (71335-1102-1)
- ndc11713351102290 TABLET, FILM COATED in 1 BOTTLE (71335-1102-2)
- ndc11713351102360 TABLET, FILM COATED in 1 BOTTLE (71335-1102-3)
- ndc117133511024120 TABLET, FILM COATED in 1 BOTTLE (71335-1102-4)
- ndc117133511025100 TABLET, FILM COATED in 1 BOTTLE (71335-1102-5)
- ndc117133511026180 TABLET, FILM COATED in 1 BOTTLE (71335-1102-6)
- ndc11713351102710 TABLET, FILM COATED in 1 BOTTLE (71335-1102-7)
- ndc1171335110287 TABLET, FILM COATED in 1 BOTTLE (71335-1102-8)
Annotations
UNII (FDA Substance ID)
3ST302B24A
LOSARTAN POTASSIUM
RxCUI 203160
Orange Book
A203835
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": "71335-1102_ee7edcfc-8787-49ba-810c-6c4f5d5fa8df",
"productndc": "71335-1102",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "203835",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "25MG",
"product_no": "001",
"approval_date": "Aug 12, 2015"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "50MG",
"product_no": "002",
"approval_date": "Aug 12, 2015"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "100MG",
"product_no": "003",
"approval_date": "Aug 12, 2015"
}
],
"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": "ANDA203835",
"marketing_category": "ANDA",
"nonproprietary_name": "Losartan Potassium",
"start_marketing_date": "20150819",
"active_numerator_strength": "50"
}Related drugs
Other records sharing ATC code C09CA01.
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