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United States · US · US:71205-239_0ca67162-b529-4986-bf16-a57ca3af0103

Prednisone

Orange BookUNIISPLATC A07EA03

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

Identification

ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeA07EA03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 13

  • ndc11
    7120523905
    5 TABLET in 1 BOTTLE (71205-239-05)
  • ndc11
    7120523906
    6 TABLET in 1 BOTTLE (71205-239-06)
  • ndc11
    7120523907
    7 TABLET in 1 BOTTLE (71205-239-07)
  • ndc11
    7120523910
    10 TABLET in 1 BOTTLE (71205-239-10)
  • ndc11
    7120523912
    12 TABLET in 1 BOTTLE (71205-239-12)
  • ndc11
    7120523914
    14 TABLET in 1 BOTTLE (71205-239-14)
  • ndc11
    7120523915
    15 TABLET in 1 BOTTLE (71205-239-15)
  • ndc11
    7120523918
    18 TABLET in 1 BOTTLE (71205-239-18)
  • ndc11
    7120523920
    20 TABLET in 1 BOTTLE (71205-239-20)
  • ndc11
    7120523921
    21 TABLET in 1 BOTTLE (71205-239-21)
  • ndc11
    7120523930
    30 TABLET in 1 BOTTLE (71205-239-30)
  • ndc11
    7120523960
    60 TABLET in 1 BOTTLE (71205-239-60)
  • ndc11
    7120523990
    90 TABLET in 1 BOTTLE (71205-239-90)

Annotations

UNII (FDA Substance ID)
VB0R961HZT
PREDNISONE
RxCUI 8640
Orange Book
A085161
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "VB0R961HZT",
    "rxcui": "8640",
    "inchikey": "XOFYZVNMUHMLCC-ZPOLXVRWSA-N",
    "display_name": "PREDNISONE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "ecc48869-3812-4440-a398-749b28062059": {
      "match": "brand_token",
      "title": "PREDNISONE TABLET [BRYANT RANCH PREPACK]",
      "spl_version": "105",
      "published_date": "2026-06-01"
    }
  },
  "productid": "71205-239_0ca67162-b529-4986-bf16-a57ca3af0103",
  "productndc": "71205-239",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "085161",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "001",
        "approval_date": "Approved Prior to Jan 1, 1982"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PREDNISONE",
  "proprietary_name": "Prednisone",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA085161",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Prednisone",
  "start_marketing_date": "19900101",
  "active_numerator_strength": "20"
}

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