OLMESARTAN MEDOXOMIL

Orange BookUNIISPLATC C09CA08

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

Identification

ManufacturerMicro Labs Limited

CountryUS (United States)

ATC codeC09CA08

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 5

ndc11
4257120205
500 TABLET, FILM COATED in 1 BOTTLE (42571-202-05)
ndc11
4257120210
1000 TABLET, FILM COATED in 1 BOTTLE (42571-202-10)
ndc11
4257120211
10 BLISTER PACK in 1 CARTON (42571-202-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42571-202-32)
ndc11
4257120230
30 TABLET, FILM COATED in 1 BOTTLE (42571-202-30)
ndc11
4257120290
90 TABLET, FILM COATED in 1 BOTTLE (42571-202-90)

Annotations

UNII (FDA Substance ID)

6M97XTV3HD

OLMESARTAN MEDOXOMIL

RxCUI 118463

Orange Book

A206372

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": "42571-202_3619c2a8-fac7-3b89-e063-6294a90a7209",
  "productndc": "42571-202",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "206372",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Sep 17, 2019"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "002",
        "approval_date": "Sep 17, 2019"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "003",
        "approval_date": "Sep 17, 2019"
      }
    ],
    "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": "ANDA206372",
  "marketing_category": "ANDA",
  "nonproprietary_name": "olmesartan medoxomil",
  "start_marketing_date": "20200203",
  "active_numerator_strength": "20"
}

Related drugs

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