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United States · US · US:71335-2530_53ee1e74-4125-4759-9ea2-a57b00544040

Diclofenac Potassium

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
    7133525301
    20 TABLET, FILM COATED in 1 BOTTLE (71335-2530-1)
  • ndc11
    7133525302
    90 TABLET, FILM COATED in 1 BOTTLE (71335-2530-2)
  • ndc11
    7133525303
    30 TABLET, FILM COATED in 1 BOTTLE (71335-2530-3)
  • ndc11
    7133525304
    60 TABLET, FILM COATED in 1 BOTTLE (71335-2530-4)
  • ndc11
    7133525305
    45 TABLET, FILM COATED in 1 BOTTLE (71335-2530-5)
  • ndc11
    7133525306
    58 TABLET, FILM COATED in 1 BOTTLE (71335-2530-6)
  • ndc11
    7133525307
    18 TABLET, FILM COATED in 1 BOTTLE (71335-2530-7)
  • ndc11
    7133525308
    120 TABLET, FILM COATED in 1 BOTTLE (71335-2530-8)
  • ndc11
    7133525309
    100 TABLET, FILM COATED in 1 BOTTLE (71335-2530-9)

Annotations

UNII (FDA Substance ID)
L4D5UA6CB4
DICLOFENAC POTASSIUM
RxCUI 81997
Orange Book
A215585
AB
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": "71335-2530_53ee1e74-4125-4759-9ea2-a57b00544040",
  "productndc": "71335-2530",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "215585",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "001",
        "approval_date": "Oct 8, 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": "ANDA215585",
  "marketing_category": "ANDA",
  "nonproprietary_name": "diclofenac potassium",
  "start_marketing_date": "20211011",
  "active_numerator_strength": "50"
}

Related drugs

Other records sharing ATC code M01AB55.

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