Dexamethasone

In shortageOrange BookUNIISPLATC A01AC02

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeA01AC02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 10

ndc11
6362937420
4 TABLET in 1 BOTTLE (63629-3742-0)
ndc11
6362937421
30 TABLET in 1 BOTTLE (63629-3742-1)
ndc11
6362937422
6 TABLET in 1 BOTTLE (63629-3742-2)
ndc11
6362937423
3 TABLET in 1 BOTTLE (63629-3742-3)
ndc11
6362937424
15 TABLET in 1 BOTTLE (63629-3742-4)
ndc11
6362937425
40 TABLET in 1 BOTTLE (63629-3742-5)
ndc11
6362937426
60 TABLET in 1 BOTTLE (63629-3742-6)
ndc11
6362937427
28 TABLET in 1 BOTTLE (63629-3742-7)
ndc11
6362937428
90 TABLET in 1 BOTTLE (63629-3742-8)
ndc11
6362937429
10 TABLET in 1 BOTTLE (63629-3742-9)

Annotations

UNII (FDA Substance ID)

7S5I7G3JQL

DEXAMETHASONE

RxCUI 3264

Orange Book

A084612

ABABABABABABAB

DailyMed SPL labels

1 version tracked

FDA shortage

Currently in shortage

Dexamethasone Sodium Phosphate Injection

Raw payload (JSON)

{
  "unii": {
    "unii": "7S5I7G3JQL",
    "rxcui": "3264",
    "inchikey": "UREBDLICKHMUKA-CXSFZGCWSA-N",
    "display_name": "DEXAMETHASONE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "bf8acfdb-8dc8-4a69-90b0-33c680c421d6": {
      "match": "brand_token",
      "title": "DEXAMETHASONE TABLET [CARDINAL HEALTH 107, LLC]",
      "spl_version": "15",
      "published_date": "2026-05-25"
    }
  },
  "productid": "63629-3742_ce3eeaa7-3b4f-455a-ae01-f592db862382",
  "productndc": "63629-3742",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "084612",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "4MG",
        "product_no": "001",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "0.5MG",
        "product_no": "002",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "0.75MG",
        "product_no": "003",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "1MG",
        "product_no": "004",
        "approval_date": "Sep 15, 1983"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "1.5MG",
        "product_no": "005",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "2MG",
        "product_no": "006",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "6MG",
        "product_no": "007",
        "approval_date": "Sep 15, 1983"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DEXAMETHASONE",
  "shortage_reason": "Dexamethasone Sodium Phosphate Injection",
  "shortage_status": "current",
  "proprietary_name": "Dexamethasone",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA084612",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Dexamethasone",
  "start_marketing_date": "19780719",
  "active_numerator_strength": "4"
}

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