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United States · US · US:62332-133_95e8d157-e834-4d1d-9520-8ee05f8ca69b

Olmesartan Medoxomil

Orange BookUNIISPLATC C09CA08

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

Identification

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

Packs · 4

  • ndc11
    6233213310
    100 TABLET, FILM COATED in 1 CARTON (62332-133-10)
  • ndc11
    6233213330
    30 TABLET, FILM COATED in 1 BOTTLE (62332-133-30)
  • ndc11
    6233213390
    90 TABLET, FILM COATED in 1 BOTTLE (62332-133-90)
  • ndc11
    6233213391
    1000 TABLET, FILM COATED in 1 BOTTLE (62332-133-91)

Annotations

UNII (FDA Substance ID)
6M97XTV3HD
OLMESARTAN MEDOXOMIL
RxCUI 118463
Orange Book
A203012
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": "62332-133_95e8d157-e834-4d1d-9520-8ee05f8ca69b",
  "productndc": "62332-133",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "203012",
    "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": "ANDA203012",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Olmesartan Medoxomil",
  "start_marketing_date": "20170424",
  "active_numerator_strength": "40"
}

Related drugs

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