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United States · US · US:72789-374_31f654da-06fe-9e86-e063-6294a90a3312

SULINDAC

Orange BookUNIISPLATC M01AB02

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

Identification

ManufacturerPD-Rx Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeM01AB02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    7278937401
    100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01)
  • ndc11
    7278937482
    500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82)

Annotations

UNII (FDA Substance ID)
184SNS8VUH
SULINDAC
RxCUI 10237
Orange Book
A072051
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "184SNS8VUH",
    "rxcui": "10237",
    "inchikey": "MLKXDPUZXIRXEP-MFOYZWKCSA-N",
    "display_name": "SULINDAC",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "6041acc2-5e8a-4d3c-bf50-7e9447748e2b": {
      "match": "brand_token",
      "title": "SULINDAC TABLET [A-S MEDICATION SOLUTIONS]",
      "spl_version": "16",
      "published_date": "2026-05-11"
    }
  },
  "productid": "72789-374_31f654da-06fe-9e86-e063-6294a90a3312",
  "productndc": "72789-374",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "072051",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "200MG",
        "product_no": "001",
        "approval_date": "Apr 17, 1991"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "SULINDAC",
  "proprietary_name": "SULINDAC",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA072051",
  "marketing_category": "ANDA",
  "nonproprietary_name": "sulindac",
  "start_marketing_date": "20090904",
  "active_numerator_strength": "200"
}

Related drugs

Other records sharing ATC code M01AB02.

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