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United States · US · US:67877-446_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 · 8

  • ndc11
    6787744605
    500 TABLET, COATED in 1 BOTTLE (67877-446-05)
  • ndc11
    6787744610
    1000 TABLET, COATED in 1 BOTTLE (67877-446-10)
  • ndc11
    6787744630
    30 TABLET, COATED in 1 BOTTLE (67877-446-30)
  • ndc11
    6787744633
    1 BLISTER PACK in 1 CARTON (67877-446-33) / 10 TABLET, COATED in 1 BLISTER PACK
  • ndc11
    6787744638
    10 BLISTER PACK in 1 CARTON (67877-446-38) / 10 TABLET, COATED in 1 BLISTER PACK
  • ndc11
    6787744674
    5 BLISTER PACK in 1 CARTON (67877-446-74) / 10 TABLET, COATED in 1 BLISTER PACK
  • ndc11
    6787744684
    3 BLISTER PACK in 1 CARTON (67877-446-84) / 10 TABLET, COATED in 1 BLISTER PACK
  • ndc11
    6787744690
    90 TABLET, COATED in 1 BOTTLE (67877-446-90)

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": "67877-446_a1d66aa9-d0fa-4d21-bba0-ff8078c2e5af",
  "productndc": "67877-446",
  "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": "20"
}

Related drugs

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