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United States · US · US:71335-2079_2a5ad2f0-8a26-4514-8498-a66afc78d169
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
- ndc11713352079011 TABLET in 1 BOTTLE, PLASTIC (71335-2079-0)
- ndc11713352079120 TABLET in 1 BOTTLE, PLASTIC (71335-2079-1)
- ndc11713352079230 TABLET in 1 BOTTLE, PLASTIC (71335-2079-2)
- ndc11713352079340 TABLET in 1 BOTTLE, PLASTIC (71335-2079-3)
- ndc11713352079415 TABLET in 1 BOTTLE, PLASTIC (71335-2079-4)
- ndc11713352079510 TABLET in 1 BOTTLE, PLASTIC (71335-2079-5)
- ndc11713352079621 TABLET in 1 BOTTLE, PLASTIC (71335-2079-6)
- ndc11713352079718 TABLET in 1 BOTTLE, PLASTIC (71335-2079-7)
- ndc11713352079812 TABLET in 1 BOTTLE, PLASTIC (71335-2079-8)
- ndc11713352079923 TABLET in 1 BOTTLE, PLASTIC (71335-2079-9)
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": "71335-2079_2a5ad2f0-8a26-4514-8498-a66afc78d169",
"productndc": "71335-2079",
"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": "20"
}Related drugs
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- 🇮🇹CISON*20 cpr 5 mgGENETIC SpA
- 🇫🇷CORTANCYL 1 mg, compriméCHEPLAPHARM ARZNEIMITTEL (ALLEMAGNE)
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- 🇮🇹CORTIREX*20 cpr 20 mgFARTO Srl
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