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United States · US · US:63629-4108_37d9b7c1-4bf8-44ed-8d48-bd1ee6efd72c

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 · 8

  • ndc11
    6362941081
    20 TABLET, FILM COATED in 1 BOTTLE (63629-4108-1)
  • ndc11
    6362941082
    90 TABLET, FILM COATED in 1 BOTTLE (63629-4108-2)
  • ndc11
    6362941083
    30 TABLET, FILM COATED in 1 BOTTLE (63629-4108-3)
  • ndc11
    6362941084
    60 TABLET, FILM COATED in 1 BOTTLE (63629-4108-4)
  • ndc11
    6362941085
    45 TABLET, FILM COATED in 1 BOTTLE (63629-4108-5)
  • ndc11
    6362941086
    58 TABLET, FILM COATED in 1 BOTTLE (63629-4108-6)
  • ndc11
    6362941087
    18 TABLET, FILM COATED in 1 BOTTLE (63629-4108-7)
  • ndc11
    6362941088
    120 TABLET, FILM COATED in 1 BOTTLE (63629-4108-8)

Annotations

UNII (FDA Substance ID)
L4D5UA6CB4
DICLOFENAC POTASSIUM
RxCUI 81997
Orange Book
A075219
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": "63629-4108_37d9b7c1-4bf8-44ed-8d48-bd1ee6efd72c",
  "productndc": "63629-4108",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "075219",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "001",
        "approval_date": "Aug 6, 1998"
      }
    ],
    "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": "ANDA075219",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Diclofenac Potassium",
  "start_marketing_date": "19980811",
  "active_numerator_strength": "50"
}

Related drugs

Other records sharing ATC code M01AB55.

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