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United States · US · US:68462-437_3d590efe-ccb3-4ca3-b49e-9547dd674eae

Olmesartan Medoxomil

Orange BookUNIISPLATC C09CA08

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

Identification

ManufacturerGlenmark Pharmaceuticals Inc., USA
CountryUS (United States)
ATC codeC09CA08
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    6846243710
    1000 TABLET, FILM COATED in 1 BOTTLE (68462-437-10)
  • ndc11
    6846243711
    10 BLISTER PACK in 1 CARTON (68462-437-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    6846243730
    30 TABLET, FILM COATED in 1 BOTTLE (68462-437-30)
  • ndc11
    6846243790
    90 TABLET, FILM COATED in 1 BOTTLE (68462-437-90)

Annotations

UNII (FDA Substance ID)
6M97XTV3HD
OLMESARTAN MEDOXOMIL
RxCUI 118463
Orange Book
A203281
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": "68462-437_3d590efe-ccb3-4ca3-b49e-9547dd674eae",
  "productndc": "68462-437",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "203281",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "May 25, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "002",
        "approval_date": "May 25, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "003",
        "approval_date": "May 25, 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": "ANDA203281",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Olmesartan Medoxomil",
  "start_marketing_date": "20170525",
  "active_numerator_strength": "20"
}

Related drugs

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