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United States · US · US:67877-447_a1d66aa9-d0fa-4d21-bba0-ff8078c2e5af

Olmesartan Medoxomil

Orange BookUNIISPLATC C09CA08

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

Identification

ManufacturerAscend Laboratories, LLC
CountryUS (United States)
ATC codeC09CA08
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    6787744705
    500 TABLET, COATED in 1 BOTTLE (67877-447-05)
  • ndc11
    6787744710
    1000 TABLET, COATED in 1 BOTTLE (67877-447-10)
  • ndc11
    6787744730
    30 TABLET, COATED in 1 BOTTLE (67877-447-30)
  • ndc11
    6787744790
    90 TABLET, COATED in 1 BOTTLE (67877-447-90)

Annotations

UNII (FDA Substance ID)
6M97XTV3HD
OLMESARTAN MEDOXOMIL
RxCUI 118463
Orange Book
A206763
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": "67877-447_a1d66aa9-d0fa-4d21-bba0-ff8078c2e5af",
  "productndc": "67877-447",
  "dosage_form": "TABLET, COATED",
  "orange_book": {
    "appl_no": "206763",
    "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": "ANDA206763",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Olmesartan Medoxomil",
  "start_marketing_date": "20170424",
  "active_numerator_strength": "40"
}

Related drugs

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