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United States · US · US:33342-045_81824d1f-61f4-457c-8723-cd43d5429029

Losartan potassium

Orange BookUNIISPLATC C09CA01

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerMacleods Pharmaceuticals Limited
CountryUS (United States)
ATC codeC09CA01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    3334204507
    30 TABLET, FILM COATED in 1 BOTTLE (33342-045-07)
  • ndc11
    3334204510
    90 TABLET, FILM COATED in 1 BOTTLE (33342-045-10)
  • ndc11
    3334204512
    10 BLISTER PACK in 1 CARTON (33342-045-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    3334204544
    1000 TABLET, FILM COATED in 1 BOTTLE (33342-045-44)

Annotations

UNII (FDA Substance ID)
3ST302B24A
LOSARTAN POTASSIUM
RxCUI 203160
Orange Book
A202230
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": "33342-045_81824d1f-61f4-457c-8723-cd43d5429029",
  "productndc": "33342-045",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "202230",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "25MG",
        "product_no": "001",
        "approval_date": "May 30, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "002",
        "approval_date": "May 30, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "003",
        "approval_date": "May 30, 2012"
      }
    ],
    "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": "ANDA202230",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Losartan potassium",
  "start_marketing_date": "20120601",
  "active_numerator_strength": "50"
}

Related drugs

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