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United States · US · US:71335-0648_cfa0cb80-a307-440c-99c4-88576c0c8bdb

Diclofenac Sodium

Orange BookUNIISPLATC M01AB55

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeM01AB55
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 9

  • ndc11
    7133506481
    60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-1)
  • ndc11
    7133506482
    30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-2)
  • ndc11
    7133506483
    15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-3)
  • ndc11
    7133506484
    14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-4)
  • ndc11
    7133506485
    10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-5)
  • ndc11
    7133506486
    21 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-6)
  • ndc11
    7133506487
    90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-7)
  • ndc11
    7133506488
    120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-8)
  • ndc11
    7133506489
    7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-9)

Annotations

UNII (FDA Substance ID)
QTG126297Q
DICLOFENAC SODIUM
RxCUI 203214
Orange Book
A075492
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "QTG126297Q",
    "rxcui": "203214",
    "inchikey": "KPHWPUGNDIVLNH-UHFFFAOYSA-M",
    "display_name": "DICLOFENAC SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "86461915-9bc1-43d4-8d92-6eef3e56bd90": {
      "match": "brand_token",
      "title": "DICLOFENAC POTASSIUM TABLET, COATED [BRYANT RANCH PREPACK]",
      "spl_version": "104",
      "published_date": "2026-06-01"
    }
  },
  "productid": "71335-0648_cfa0cb80-a307-440c-99c4-88576c0c8bdb",
  "productndc": "71335-0648",
  "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "075492",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "001",
        "approval_date": "Feb 11, 2000"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DICLOFENAC SODIUM",
  "proprietary_name": "Diclofenac Sodium",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA075492",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Diclofenac Sodium",
  "start_marketing_date": "20000228",
  "active_numerator_strength": "100"
}

Related drugs

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