olmesartan medoxomil

Orange BookUNIISPLATC C09CA08

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

Identification

ManufacturerAccord Healthcare Inc.

CountryUS (United States)

ATC codeC09CA08

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
1672932210
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-10)
ndc11
1672932215
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-15)
ndc11
1672932217
1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-17)

Annotations

UNII (FDA Substance ID)

6M97XTV3HD

OLMESARTAN MEDOXOMIL

RxCUI 118463

Orange Book

A207662

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": "16729-322_424dbf67-5be3-2810-e063-6294a90a3558",
  "productndc": "16729-322",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "207662",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Apr 24, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "002",
        "approval_date": "Apr 24, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "003",
        "approval_date": "Apr 24, 2017"
      }
    ],
    "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": "ANDA207662",
  "marketing_category": "ANDA",
  "nonproprietary_name": "olmesartan medoxomil",
  "start_marketing_date": "20170427",
  "active_numerator_strength": "40"
}

Related drugs

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