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United States · US · US:71335-1817_fb077532-f94e-44e1-afd3-6be55c4062c8

Losartan potassium Tablets, 50 mg

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
    7133518171
    30 TABLET in 1 BOTTLE (71335-1817-1)
  • ndc11
    7133518172
    90 TABLET in 1 BOTTLE (71335-1817-2)
  • ndc11
    7133518173
    60 TABLET in 1 BOTTLE (71335-1817-3)
  • ndc11
    7133518174
    120 TABLET in 1 BOTTLE (71335-1817-4)
  • ndc11
    7133518175
    100 TABLET in 1 BOTTLE (71335-1817-5)
  • ndc11
    7133518176
    180 TABLET in 1 BOTTLE (71335-1817-6)
  • ndc11
    7133518177
    10 TABLET in 1 BOTTLE (71335-1817-7)
  • ndc11
    7133518178
    7 TABLET in 1 BOTTLE (71335-1817-8)

Annotations

UNII (FDA Substance ID)
3ST302B24A
LOSARTAN POTASSIUM
RxCUI 203160
Orange Book
A201170
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": "71335-1817_fb077532-f94e-44e1-afd3-6be55c4062c8",
  "productndc": "71335-1817",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "201170",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "25MG",
        "product_no": "001",
        "approval_date": "Sep 18, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "002",
        "approval_date": "Sep 18, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "003",
        "approval_date": "Sep 18, 2012"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LOSARTAN POTASSIUM",
  "proprietary_name": "Losartan potassium Tablets, 50 mg",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA201170",
  "marketing_category": "ANDA",
  "nonproprietary_name": "losartan potassium",
  "start_marketing_date": "20120918",
  "active_numerator_strength": "50"
}

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