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United States · US · US:71335-1238_72d96aa7-bd3d-44e0-98cf-b65a738221d9

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
    7133512381
    60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1238-1)
  • ndc11
    7133512382
    30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1238-2)
  • ndc11
    7133512383
    15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1238-3)
  • ndc11
    7133512384
    14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1238-4)
  • ndc11
    7133512385
    10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1238-5)
  • ndc11
    7133512386
    21 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1238-6)
  • ndc11
    7133512387
    90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1238-7)
  • ndc11
    7133512388
    120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1238-8)
  • ndc11
    7133512389
    7 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1238-9)

Annotations

UNII (FDA Substance ID)
QTG126297Q
DICLOFENAC SODIUM
RxCUI 203214
Orange Book
A076201
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": "71335-1238_72d96aa7-bd3d-44e0-98cf-b65a738221d9",
  "productndc": "71335-1238",
  "dosage_form": "TABLET, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "076201",
    "products": [
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "001",
        "approval_date": "Nov 6, 2002"
      }
    ],
    "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": "ANDA076201",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Diclofenac Sodium",
  "start_marketing_date": "20021106",
  "active_numerator_strength": "100"
}

Related drugs

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