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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

  • ndc11
    7133511021
    30 TABLET, FILM COATED in 1 BOTTLE (71335-1102-1)
  • ndc11
    7133511022
    90 TABLET, FILM COATED in 1 BOTTLE (71335-1102-2)
  • ndc11
    7133511023
    60 TABLET, FILM COATED in 1 BOTTLE (71335-1102-3)
  • ndc11
    7133511024
    120 TABLET, FILM COATED in 1 BOTTLE (71335-1102-4)
  • ndc11
    7133511025
    100 TABLET, FILM COATED in 1 BOTTLE (71335-1102-5)
  • ndc11
    7133511026
    180 TABLET, FILM COATED in 1 BOTTLE (71335-1102-6)
  • ndc11
    7133511027
    10 TABLET, FILM COATED in 1 BOTTLE (71335-1102-7)
  • ndc11
    7133511028
    7 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"
}

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