Prednisone

Orange BookUNIISPLATC A07EA03

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

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
7133503350
10 TABLET in 1 BOTTLE (71335-0335-0)
ndc11
7133503351
21 TABLET in 1 BOTTLE (71335-0335-1)
ndc11
7133503352
40 TABLET in 1 BOTTLE (71335-0335-2)
ndc11
7133503353
30 TABLET in 1 BOTTLE (71335-0335-3)
ndc11
7133503354
20 TABLET in 1 BOTTLE (71335-0335-4)
ndc11
7133503355
15 TABLET in 1 BOTTLE (71335-0335-5)
ndc11
7133503356
50 TABLET in 1 BOTTLE (71335-0335-6)
ndc11
7133503357
60 TABLET in 1 BOTTLE (71335-0335-7)
ndc11
7133503358
42 TABLET in 1 BOTTLE (71335-0335-8)
ndc11
7133503359
48 TABLET in 1 BOTTLE (71335-0335-9)

Annotations

UNII (FDA Substance ID)

VB0R961HZT

PREDNISONE

RxCUI 8640

Orange Book

A040362

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": "71335-0335_1d5b8df8-e31d-4c84-ab41-46c718ebb027",
  "productndc": "71335-0335",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "040362",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Aug 29, 2001"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "002",
        "approval_date": "Aug 29, 2001"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "003",
        "approval_date": "Jun 29, 2005"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "2.5MG",
        "product_no": "004",
        "approval_date": "Apr 17, 2023"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "005",
        "approval_date": "Apr 17, 2023"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PREDNISONE",
  "proprietary_name": "Prednisone",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA040362",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Prednisone",
  "start_marketing_date": "20010829",
  "active_numerator_strength": "10"
}

Related drugs

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