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United States · US · US:68788-7315_dc20bec2-e885-442a-93bb-2de09faa44c9

Etodolac

Orange BookUNIISPLATC M01AB08

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

Identification

ManufacturerPreferred Pharmaceuticals Inc.
CountryUS (United States)
ATC codeM01AB08
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 5

  • ndc11
    6878873151
    100 TABLET, FILM COATED in 1 BOTTLE (68788-7315-1)
  • ndc11
    6878873152
    20 TABLET, FILM COATED in 1 BOTTLE (68788-7315-2)
  • ndc11
    6878873153
    30 TABLET, FILM COATED in 1 BOTTLE (68788-7315-3)
  • ndc11
    6878873156
    60 TABLET, FILM COATED in 1 BOTTLE (68788-7315-6)
  • ndc11
    6878873159
    90 TABLET, FILM COATED in 1 BOTTLE (68788-7315-9)

Annotations

UNII (FDA Substance ID)
2M36281008
ETODOLAC
RxCUI 24605
Orange Book
A208834
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "2M36281008",
    "rxcui": "24605",
    "inchikey": "NNYBQONXHNTVIJ-UHFFFAOYSA-N",
    "display_name": "ETODOLAC",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "007c55fa-ef8b-4a8e-bfe5-e47c6e5da727": {
      "match": "brand_token",
      "title": "ETODOLAC TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]",
      "spl_version": "26",
      "published_date": "2026-05-25"
    }
  },
  "productid": "68788-7315_dc20bec2-e885-442a-93bb-2de09faa44c9",
  "productndc": "68788-7315",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "208834",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "400MG",
        "product_no": "001",
        "approval_date": "Jun 7, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "500MG",
        "product_no": "002",
        "approval_date": "Jun 7, 2018"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ETODOLAC",
  "proprietary_name": "Etodolac",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA208834",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Etodolac",
  "start_marketing_date": "20190102",
  "active_numerator_strength": "400"
}

Related drugs

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