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United States · US · US:71335-0456_824033ce-a50b-4914-b0b9-b0005739555c

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 · 10

  • ndc11
    7133504560
    40 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-0)
  • ndc11
    7133504561
    28 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-1)
  • ndc11
    7133504562
    60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-2)
  • ndc11
    7133504563
    20 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-3)
  • ndc11
    7133504564
    30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-4)
  • ndc11
    7133504565
    120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-5)
  • ndc11
    7133504566
    90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-6)
  • ndc11
    7133504567
    100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-7)
  • ndc11
    7133504568
    15 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-8)
  • ndc11
    7133504569
    14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-9)

Annotations

UNII (FDA Substance ID)
QTG126297Q
DICLOFENAC SODIUM
RxCUI 203214
Orange Book
A077863
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": "71335-0456_824033ce-a50b-4914-b0b9-b0005739555c",
  "productndc": "71335-0456",
  "dosage_form": "TABLET, DELAYED RELEASE",
  "orange_book": {
    "appl_no": "077863",
    "products": [
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "75MG",
        "product_no": "003",
        "approval_date": "Jun 8, 2007"
      }
    ],
    "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": "ANDA077863",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Diclofenac Sodium",
  "start_marketing_date": "20080819",
  "active_numerator_strength": "75"
}

Related drugs

Other records sharing ATC code M01AB55.

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