Losartan Potassium

Orange BookUNIISPLATC C09CA01

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeC09CA01

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 7

ndc11
7133502621
30 TABLET, FILM COATED in 1 BOTTLE (71335-0262-1)
ndc11
7133502622
90 TABLET, FILM COATED in 1 BOTTLE (71335-0262-2)
ndc11
7133502623
60 TABLET, FILM COATED in 1 BOTTLE (71335-0262-3)
ndc11
7133502624
120 TABLET, FILM COATED in 1 BOTTLE (71335-0262-4)
ndc11
7133502625
100 TABLET, FILM COATED in 1 BOTTLE (71335-0262-5)
ndc11
7133502626
180 TABLET, FILM COATED in 1 BOTTLE (71335-0262-6)
ndc11
7133502627
10 TABLET, FILM COATED in 1 BOTTLE (71335-0262-7)

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": "71335-0262_570fae9a-6e7f-4704-8ca0-12aa2e12f3e0",
  "productndc": "71335-0262",
  "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": "50"
}

Related drugs

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