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United States · US · US:63187-066_c1b5fac9-ec3d-491f-8e58-bba1d0f9d861

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 · 12

  • ndc11
    6318706605
    5 TABLET in 1 BOTTLE (63187-066-05)
  • ndc11
    6318706606
    6 TABLET in 1 BOTTLE (63187-066-06)
  • ndc11
    6318706608
    8 TABLET in 1 BOTTLE (63187-066-08)
  • ndc11
    6318706609
    9 TABLET in 1 BOTTLE (63187-066-09)
  • ndc11
    6318706612
    12 TABLET in 1 BOTTLE (63187-066-12)
  • ndc11
    6318706615
    15 TABLET in 1 BOTTLE (63187-066-15)
  • ndc11
    6318706620
    20 TABLET in 1 BOTTLE (63187-066-20)
  • ndc11
    6318706621
    21 TABLET in 1 BOX, UNIT-DOSE (63187-066-21)
  • ndc11
    6318706624
    24 TABLET in 1 BOTTLE (63187-066-24)
  • ndc11
    6318706630
    30 TABLET in 1 BOTTLE (63187-066-30)
  • ndc11
    6318706640
    40 TABLET in 1 BOTTLE (63187-066-40)
  • ndc11
    6318706642
    42 TABLET in 1 BOTTLE (63187-066-42)

Annotations

UNII (FDA Substance ID)
VB0R961HZT
PREDNISONE
RxCUI 8640
Orange Book
A040256
ABAB
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": "63187-066_c1b5fac9-ec3d-491f-8e58-bba1d0f9d861",
  "productndc": "63187-066",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "040256",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Jul 12, 2002"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Jul 12, 2002"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PREDNISONE",
  "proprietary_name": "Prednisone",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA040256",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Prednisone",
  "start_marketing_date": "20020712",
  "active_numerator_strength": "5"
}

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