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United States · US · US:63629-1605_aeb416b3-5b23-47cc-9c0e-2aae45798f94

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
    6362916050
    42 TABLET in 1 BOTTLE (63629-1605-0)
  • ndc11
    6362916051
    30 TABLET in 1 BOTTLE (63629-1605-1)
  • ndc11
    6362916052
    78 TABLET in 1 BOTTLE (63629-1605-2)
  • ndc11
    6362916053
    36 TABLET in 1 BOTTLE (63629-1605-3)
  • ndc11
    6362916054
    21 TABLET in 1 BOTTLE (63629-1605-4)
  • ndc11
    6362916055
    15 TABLET in 1 BOTTLE (63629-1605-5)
  • ndc11
    6362916056
    100 TABLET in 1 BOTTLE (63629-1605-6)
  • ndc11
    6362916057
    20 TABLET in 1 BOTTLE (63629-1605-7)
  • ndc11
    6362916058
    10 TABLET in 1 BOTTLE (63629-1605-8)
  • ndc11
    6362916059
    90 TABLET in 1 BOTTLE (63629-1605-9)

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": "63629-1605_aeb416b3-5b23-47cc-9c0e-2aae45798f94",
  "productndc": "63629-1605",
  "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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