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United States · US · US:68788-8639_0cf5c1aa-fe22-4d4f-91d1-e8706975f44e

Losortan Potassium

Orange BookUNIISPLATC C09CA01

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

Identification

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

Packs · 5

  • ndc11
    6878886391
    100 TABLET, FILM COATED in 1 BOTTLE (68788-8639-1)
  • ndc11
    6878886393
    30 TABLET, FILM COATED in 1 BOTTLE (68788-8639-3)
  • ndc11
    6878886395
    50 TABLET, FILM COATED in 1 BOTTLE (68788-8639-5)
  • ndc11
    6878886396
    60 TABLET, FILM COATED in 1 BOTTLE (68788-8639-6)
  • ndc11
    6878886399
    90 TABLET, FILM COATED in 1 BOTTLE (68788-8639-9)

Annotations

UNII (FDA Substance ID)
3ST302B24A
LOSARTAN POTASSIUM
RxCUI 203160
Orange Book
A078243
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": {
    "25651749-8950-43ff-bcbd-3bb85f57a360": {
      "match": "brand_token",
      "title": "LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.]",
      "spl_version": "3",
      "published_date": "2026-06-01"
    }
  },
  "productid": "68788-8639_0cf5c1aa-fe22-4d4f-91d1-e8706975f44e",
  "productndc": "68788-8639",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "078243",
    "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": "Losortan Potassium",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA078243",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Losartan Potassium",
  "start_marketing_date": "20240418",
  "active_numerator_strength": "25"
}

Related drugs

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