Diclofenac Potassium

Orange BookUNIISPLATC M01AB55

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

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
7133520521
20 TABLET, COATED in 1 BOTTLE (71335-2052-1)
ndc11
7133520522
90 TABLET, COATED in 1 BOTTLE (71335-2052-2)
ndc11
7133520523
30 TABLET, COATED in 1 BOTTLE (71335-2052-3)
ndc11
7133520524
60 TABLET, COATED in 1 BOTTLE (71335-2052-4)
ndc11
7133520525
45 TABLET, COATED in 1 BOTTLE (71335-2052-5)
ndc11
7133520526
58 TABLET, COATED in 1 BOTTLE (71335-2052-6)
ndc11
7133520527
18 TABLET, COATED in 1 BOTTLE (71335-2052-7)
ndc11
7133520528
120 TABLET, COATED in 1 BOTTLE (71335-2052-8)
ndc11
7133520529
100 TABLET, COATED in 1 BOTTLE (71335-2052-9)

Annotations

UNII (FDA Substance ID)

L4D5UA6CB4

DICLOFENAC POTASSIUM

RxCUI 81997

Orange Book

A075229

ABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "L4D5UA6CB4",
    "rxcui": "81997",
    "inchikey": "KXZOIWWTXOCYKR-UHFFFAOYSA-M",
    "display_name": "DICLOFENAC POTASSIUM",
    "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": "71335-2052_2bb8e66c-3fab-446d-9284-e939bf8940f0",
  "productndc": "71335-2052",
  "dosage_form": "TABLET, COATED",
  "orange_book": {
    "appl_no": "075229",
    "products": [
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "001",
        "approval_date": "Nov 20, 1998"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "25MG",
        "product_no": "002",
        "approval_date": "Sep 16, 2021"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DICLOFENAC POTASSIUM",
  "proprietary_name": "Diclofenac Potassium",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA075229",
  "marketing_category": "ANDA",
  "nonproprietary_name": "diclofenac potassium",
  "start_marketing_date": "20201219",
  "active_numerator_strength": "50"
}

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