Losartan Potassium

Orange BookUNIISPLATC C09CA01

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

Identification

ManufacturerREMEDYREPACK INC.

CountryUS (United States)

ATC codeC09CA01

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 5

ndc11
7051838940
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3894-0)
ndc11
7051838941
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3894-1)
ndc11
7051838942
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3894-2)
ndc11
7051838943
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3894-3)
ndc11
7051838944
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3894-4)

Annotations

UNII (FDA Substance ID)

3ST302B24A

LOSARTAN POTASSIUM

RxCUI 203160

Orange Book

A203835

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": "70518-3894_471733cb-e09a-1fe8-e063-6394a90a09fe",
  "productndc": "70518-3894",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "203835",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "25MG",
        "product_no": "001",
        "approval_date": "Aug 12, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "002",
        "approval_date": "Aug 12, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "003",
        "approval_date": "Aug 12, 2015"
      }
    ],
    "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": "ANDA203835",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Losartan Potassium",
  "start_marketing_date": "20231016",
  "active_numerator_strength": "25"
}

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