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United States · US · US:71335-1235_2e19e89b-daac-449a-a511-217ed561f5fd

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
    7133512351
    30 TABLET, FILM COATED in 1 BOTTLE (71335-1235-1)
  • ndc11
    7133512352
    60 TABLET, FILM COATED in 1 BOTTLE (71335-1235-2)
  • ndc11
    7133512353
    90 TABLET, FILM COATED in 1 BOTTLE (71335-1235-3)
  • ndc11
    7133512354
    120 TABLET, FILM COATED in 1 BOTTLE (71335-1235-4)
  • ndc11
    7133512355
    100 TABLET, FILM COATED in 1 BOTTLE (71335-1235-5)
  • ndc11
    7133512356
    28 TABLET, FILM COATED in 1 BOTTLE (71335-1235-6)
  • ndc11
    7133512357
    10 TABLET, FILM COATED in 1 BOTTLE (71335-1235-7)
  • ndc11
    7133512358
    180 TABLET, FILM COATED in 1 BOTTLE (71335-1235-8)

Annotations

UNII (FDA Substance ID)
3ST302B24A
LOSARTAN POTASSIUM
RxCUI 203160
Orange Book
A090083
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": "71335-1235_2e19e89b-daac-449a-a511-217ed561f5fd",
  "productndc": "71335-1235",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "090083",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "25MG",
        "product_no": "001",
        "approval_date": "Oct 6, 2010"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "002",
        "approval_date": "Oct 6, 2010"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "003",
        "approval_date": "Oct 6, 2010"
      }
    ],
    "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": "ANDA090083",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Losartan Potassium",
  "start_marketing_date": "20101006",
  "active_numerator_strength": "100"
}

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