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United States · US · US:71335-2108_47ef46ae-6174-4863-8d17-303cb456d663

Dexamethasone

In shortageOrange BookUNIISPLATC A01AC02

Last synced from FDA National Drug Code directory (United States) on

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
    7133521080
    4 TABLET in 1 BOTTLE (71335-2108-0)
  • ndc11
    7133521081
    30 TABLET in 1 BOTTLE (71335-2108-1)
  • ndc11
    7133521082
    6 TABLET in 1 BOTTLE (71335-2108-2)
  • ndc11
    7133521083
    3 TABLET in 1 BOTTLE (71335-2108-3)
  • ndc11
    7133521084
    15 TABLET in 1 BOTTLE (71335-2108-4)
  • ndc11
    7133521085
    40 TABLET in 1 BOTTLE (71335-2108-5)
  • ndc11
    7133521086
    60 TABLET in 1 BOTTLE (71335-2108-6)
  • ndc11
    7133521087
    28 TABLET in 1 BOTTLE (71335-2108-7)
  • ndc11
    7133521088
    90 TABLET in 1 BOTTLE (71335-2108-8)
  • ndc11
    7133521089
    10 TABLET in 1 BOTTLE (71335-2108-9)

Annotations

UNII (FDA Substance ID)
7S5I7G3JQL
DEXAMETHASONE
RxCUI 3264
Orange Book
A088481
ABBPBPAB
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": "71335-2108_47ef46ae-6174-4863-8d17-303cb456d663",
  "productndc": "71335-2108",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "088481",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "6MG",
        "product_no": "001",
        "approval_date": "Nov 28, 1983"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "BP",
        "strength": "0.5MG",
        "product_no": "002",
        "approval_date": "Apr 28, 1983"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "BP",
        "strength": "0.75MG",
        "product_no": "003",
        "approval_date": "Apr 28, 1983"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "4MG",
        "product_no": "004",
        "approval_date": "Apr 28, 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": "ANDA088481",
  "marketing_category": "ANDA",
  "nonproprietary_name": "dexamethasone",
  "start_marketing_date": "20210628",
  "active_numerator_strength": "4"
}

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