olmesartan medoxomil

Orange BookUNIISPLATC C09CA08

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

Identification

ManufacturerREMEDYREPACK INC.

CountryUS (United States)

ATC codeC09CA08

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
7051840530
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4053-0)
ndc11
7051840531
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4053-1)
ndc11
7051840532
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4053-2)

Annotations

UNII (FDA Substance ID)

6M97XTV3HD

OLMESARTAN MEDOXOMIL

RxCUI 118463

Orange Book

A208130

ABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "6M97XTV3HD",
    "rxcui": "118463",
    "inchikey": "UQGKUQLKSCSZGY-UHFFFAOYSA-N",
    "display_name": "OLMESARTAN MEDOXOMIL",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "7f78d14a-acf2-4f82-9d20-dfcbd5e9ffb3": {
      "match": "brand_token",
      "title": "OLMESARTAN MEDOXOMIL TABLET [A-S MEDICATION SOLUTIONS]",
      "spl_version": "1",
      "published_date": "2026-06-01"
    }
  },
  "productid": "70518-4053_3fa20044-d4cd-ebda-e063-6294a90af1a2",
  "productndc": "70518-4053",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "208130",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Jun 29, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "002",
        "approval_date": "Jun 29, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "003",
        "approval_date": "Jun 29, 2018"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "OLMESARTAN MEDOXOMIL",
  "proprietary_name": "olmesartan medoxomil",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA208130",
  "marketing_category": "ANDA",
  "nonproprietary_name": "olmesartan medoxomil",
  "start_marketing_date": "20240416",
  "active_numerator_strength": "40"
}

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