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United States · US · US:71205-362_ba072b36-ff49-4d6b-b321-3fa0c73d80c5

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 · 9

  • ndc11
    7120536206
    6 TABLET in 1 BOTTLE (71205-362-06)
  • ndc11
    7120536210
    10 TABLET in 1 BOTTLE (71205-362-10)
  • ndc11
    7120536212
    12 TABLET in 1 BOTTLE (71205-362-12)
  • ndc11
    7120536215
    15 TABLET in 1 BOTTLE (71205-362-15)
  • ndc11
    7120536218
    18 TABLET in 1 BOTTLE (71205-362-18)
  • ndc11
    7120536220
    20 TABLET in 1 BOTTLE (71205-362-20)
  • ndc11
    7120536224
    24 TABLET in 1 BOTTLE (71205-362-24)
  • ndc11
    7120536228
    28 TABLET in 1 BOTTLE (71205-362-28)
  • ndc11
    7120536263
    63 TABLET in 1 BOTTLE (71205-362-63)

Annotations

UNII (FDA Substance ID)
VB0R961HZT
PREDNISONE
RxCUI 8640
Orange Book
A085162
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": "71205-362_ba072b36-ff49-4d6b-b321-3fa0c73d80c5",
  "productndc": "71205-362",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "085162",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "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": "ANDA085162",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Prednisone",
  "start_marketing_date": "19900101",
  "active_numerator_strength": "10"
}

Related drugs

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