Diclofenac Sodium

Orange BookUNIISPLATC M01AB55

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

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
7216217340
1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-0)
ndc11
7216217341
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-1)
ndc11
7216217343
30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-3)
ndc11
7216217344
20 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-4)
ndc11
7216217345
500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-5)
ndc11
7216217346
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-6)
ndc11
7216217347
14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-7)
ndc11
7216217348
15 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-8)
ndc11
7216217349
90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-9)

Annotations

UNII (FDA Substance ID)

QTG126297Q

DICLOFENAC SODIUM

RxCUI 203214

Orange Book

A075185

ABABAB

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": "72162-1734_daaf314b-5e73-4b47-895a-19f37bea7a0b",
  "productndc": "72162-1734",
  "dosage_form": "TABLET, DELAYED RELEASE",
  "orange_book": {
    "appl_no": "075185",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "75MG",
        "product_no": "001",
        "approval_date": "Nov 13, 1998"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "25MG",
        "product_no": "002",
        "approval_date": "Nov 13, 1998"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "003",
        "approval_date": "Nov 13, 1998"
      }
    ],
    "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": "ANDA075185",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Diclofenac Sodium",
  "start_marketing_date": "19981113",
  "active_numerator_strength": "75"
}

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