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United States · US · US:71335-2754_fd21957e-bea4-4025-9058-bcdd33d032ad

PredniSONE Tablets, USP, 20 mg

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
    7133527540
    11 TABLET in 1 BOTTLE (71335-2754-0)
  • ndc11
    7133527541
    20 TABLET in 1 BOTTLE (71335-2754-1)
  • ndc11
    7133527542
    30 TABLET in 1 BOTTLE (71335-2754-2)
  • ndc11
    7133527543
    40 TABLET in 1 BOTTLE (71335-2754-3)
  • ndc11
    7133527544
    15 TABLET in 1 BOTTLE (71335-2754-4)
  • ndc11
    7133527545
    10 TABLET in 1 BOTTLE (71335-2754-5)
  • ndc11
    7133527546
    21 TABLET in 1 BOTTLE (71335-2754-6)
  • ndc11
    7133527547
    18 TABLET in 1 BOTTLE (71335-2754-7)
  • ndc11
    7133527548
    12 TABLET in 1 BOTTLE (71335-2754-8)
  • ndc11
    7133527549
    23 TABLET in 1 BOTTLE (71335-2754-9)

Annotations

UNII (FDA Substance ID)
VB0R961HZT
PREDNISONE
RxCUI 8640
Orange Book
A212629
ABABAB
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": "71335-2754_fd21957e-bea4-4025-9058-bcdd33d032ad",
  "productndc": "71335-2754",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "212629",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Dec 5, 2023"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Dec 5, 2023"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "003",
        "approval_date": "Dec 5, 2023"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PREDNISONE",
  "proprietary_name": "PredniSONE Tablets, USP, 20 mg",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA212629",
  "marketing_category": "ANDA",
  "nonproprietary_name": "PredniSONE",
  "start_marketing_date": "20250522",
  "active_numerator_strength": "20"
}

Related drugs

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