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United States · US · US:62332-041_e21c14f4-6c8c-4676-b479-dff181ec3fa1

IRBESARTAN

Orange BookUNIISPLATC C09CA04

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

Identification

ManufacturerAlembic Pharmaceuticals Inc.
CountryUS (United States)
ATC codeC09CA04
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 5

  • ndc11
    6233204130
    30 TABLET in 1 BOTTLE (62332-041-30)
  • ndc11
    6233204131
    100 TABLET in 1 BOTTLE (62332-041-31)
  • ndc11
    6233204171
    500 TABLET in 1 BOTTLE (62332-041-71)
  • ndc11
    6233204190
    90 TABLET in 1 BOTTLE (62332-041-90)
  • ndc11
    6233204191
    1000 TABLET in 1 BOTTLE (62332-041-91)

Annotations

UNII (FDA Substance ID)
J0E2756Z7N
IRBESARTAN
RxCUI 83818
Orange Book
A091236
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "J0E2756Z7N",
    "rxcui": "83818",
    "inchikey": "YOSHYTLCDANDAN-UHFFFAOYSA-N",
    "display_name": "IRBESARTAN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "85494404-484c-45a1-8487-f9eb2a76490d": {
      "match": "brand_token",
      "title": "IRBESARTAN AND HYDROCHLOROTHIAZIDE TABLET [BRYANT RANCH PREPACK]",
      "spl_version": "103",
      "published_date": "2026-06-01"
    }
  },
  "productid": "62332-041_e21c14f4-6c8c-4676-b479-dff181ec3fa1",
  "productndc": "62332-041",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "091236",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "75MG",
        "product_no": "001",
        "approval_date": "Oct 15, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "150MG",
        "product_no": "002",
        "approval_date": "Oct 15, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "300MG",
        "product_no": "003",
        "approval_date": "Oct 15, 2012"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "IRBESARTAN",
  "proprietary_name": "IRBESARTAN",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA091236",
  "marketing_category": "ANDA",
  "nonproprietary_name": "IRBESARTAN",
  "start_marketing_date": "20160701",
  "active_numerator_strength": "75"
}

Related drugs

Other records sharing ATC code C09CA04.

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