VOLTAREN ARTHRITIS PAIN

Orange BookUNIISPLATC M01AB55

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

Identification

ManufacturerA-S Medication Solutions

CountryUS (United States)

ATC codeM01AB55

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5009062020
24 TUBE in 1 CASE (50090-6202-0) / 50 g in 1 TUBE

Annotations

UNII (FDA Substance ID)

QTG126297Q

DICLOFENAC SODIUM

RxCUI 203214

Orange Book

N022122

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": "TOPICAL",
  "spl_meta": {
    "30a94282-0892-442a-aa10-6525cbd4fe88": {
      "match": "brand_token",
      "title": "VOLTAREN ARTHRITIS PAIN (DICLOFENAC SODIUM) GEL VOLTAREN ARTHRITIS PAIN (DICLOFENAC SODIUM) KIT [HALEON US HOLDINGS LLC]",
      "spl_version": "13",
      "published_date": "2025-02-21"
    }
  },
  "productid": "50090-6202_46659e9a-60dd-4637-8aa4-561c48722736",
  "productndc": "50090-6202",
  "dosage_form": "GEL",
  "orange_book": {
    "appl_no": "022122",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "1%",
        "product_no": "001",
        "approval_date": "Oct 17, 2007"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DICLOFENAC SODIUM",
  "proprietary_name": "VOLTAREN ARTHRITIS PAIN",
  "active_ingred_unit": "mg/g",
  "application_number": "NDA022122",
  "marketing_category": "NDA",
  "nonproprietary_name": "diclofenac sodium",
  "start_marketing_date": "20200513",
  "active_numerator_strength": "10"
}

Related drugs

Other records sharing ATC code M01AB55.

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