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United States · US · US:71335-2122_2fb6d261-a018-44c0-883c-45f64f06ded6

prednisone

Orange BookUNIISPLATC A07EA03

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeA07EA03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 10

  • ndc11
    7133521220
    12 TABLET in 1 BOTTLE (71335-2122-0)
  • ndc11
    7133521221
    5 TABLET in 1 BOTTLE (71335-2122-1)
  • ndc11
    7133521222
    54 TABLET in 1 BOTTLE (71335-2122-2)
  • ndc11
    7133521223
    90 TABLET in 1 BOTTLE (71335-2122-3)
  • ndc11
    7133521224
    18 TABLET in 1 BOTTLE (71335-2122-4)
  • ndc11
    7133521225
    25 TABLET in 1 BOTTLE (71335-2122-5)
  • ndc11
    7133521226
    26 TABLET in 1 BOTTLE (71335-2122-6)
  • ndc11
    7133521227
    100 TABLET in 1 BOTTLE (71335-2122-7)
  • ndc11
    7133521228
    24 TABLET in 1 BOTTLE (71335-2122-8)
  • ndc11
    7133521229
    16 TABLET in 1 BOTTLE (71335-2122-9)

Annotations

UNII (FDA Substance ID)
VB0R961HZT
PREDNISONE
RxCUI 8640
Orange Book
A208412
ABABABABAB
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": "71335-2122_2fb6d261-a018-44c0-883c-45f64f06ded6",
  "productndc": "71335-2122",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "208412",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Feb 11, 2021"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "002",
        "approval_date": "Feb 11, 2021"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "003",
        "approval_date": "Jan 11, 2022"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "2.5MG",
        "product_no": "004",
        "approval_date": "Nov 20, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "005",
        "approval_date": "Nov 20, 2020"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PREDNISONE",
  "proprietary_name": "prednisone",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA208412",
  "marketing_category": "ANDA",
  "nonproprietary_name": "PREDNISONE",
  "start_marketing_date": "20210901",
  "active_numerator_strength": "10"
}

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