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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

  • ndc11
    7133520831
    30 TABLET, FILM COATED in 1 BOTTLE (71335-2083-1)
  • ndc11
    7133520832
    60 TABLET, FILM COATED in 1 BOTTLE (71335-2083-2)
  • ndc11
    7133520833
    90 TABLET, FILM COATED in 1 BOTTLE (71335-2083-3)
  • ndc11
    7133520834
    120 TABLET, FILM COATED in 1 BOTTLE (71335-2083-4)
  • ndc11
    7133520835
    100 TABLET, FILM COATED in 1 BOTTLE (71335-2083-5)
  • ndc11
    7133520836
    28 TABLET, FILM COATED in 1 BOTTLE (71335-2083-6)
  • ndc11
    7133520837
    10 TABLET, FILM COATED in 1 BOTTLE (71335-2083-7)
  • ndc11
    7133520838
    180 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

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