prednisone

Orange BookUNIISPLATC A07EA03

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

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
7120572910
10 TABLET in 1 BOTTLE, PLASTIC (71205-729-10)
ndc11
7120572914
14 TABLET in 1 BOTTLE, PLASTIC (71205-729-14)
ndc11
7120572918
18 TABLET in 1 BOTTLE, PLASTIC (71205-729-18)
ndc11
7120572920
20 TABLET in 1 BOTTLE, PLASTIC (71205-729-20)
ndc11
7120572921
21 TABLET in 1 BOTTLE, PLASTIC (71205-729-21)
ndc11
7120572928
28 TABLET in 1 BOTTLE, PLASTIC (71205-729-28)
ndc11
7120572930
30 TABLET in 1 BOTTLE, PLASTIC (71205-729-30)
ndc11
7120572940
40 TABLET in 1 BOTTLE, PLASTIC (71205-729-40)
ndc11
7120572942
42 TABLET in 1 BOTTLE, PLASTIC (71205-729-42)
ndc11
7120572960
60 TABLET in 1 BOTTLE, PLASTIC (71205-729-60)
ndc11
7120572963
63 TABLET in 1 BOTTLE, PLASTIC (71205-729-63)
ndc11
7120572990
90 TABLET in 1 BOTTLE, PLASTIC (71205-729-90)

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": "71205-729_0b164f9b-29c6-4398-8bde-7e81558809d6",
  "productndc": "71205-729",
  "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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