🇺🇸
United States · US · US:71205-755_22d9fd96-cad5-4762-9a56-0ff63357ed9e
prednisone
Orange BookUNIISPLATC A07EA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeA07EA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 15
- ndc1171205755055 TABLET in 1 BOTTLE (71205-755-05)
- ndc1171205755066 TABLET in 1 BOTTLE (71205-755-06)
- ndc1171205755077 TABLET in 1 BOTTLE (71205-755-07)
- ndc11712057551010 TABLET in 1 BOTTLE (71205-755-10)
- ndc11712057551212 TABLET in 1 BOTTLE (71205-755-12)
- ndc11712057551414 TABLET in 1 BOTTLE (71205-755-14)
- ndc11712057551515 TABLET in 1 BOTTLE (71205-755-15)
- ndc11712057551818 TABLET in 1 BOTTLE (71205-755-18)
- ndc11712057552020 TABLET in 1 BOTTLE (71205-755-20)
- ndc11712057552121 TABLET in 1 BOTTLE (71205-755-21)
- ndc11712057552424 TABLET in 1 BOTTLE (71205-755-24)
- ndc11712057552828 TABLET in 1 BOTTLE (71205-755-28)
- ndc11712057553030 TABLET in 1 BOTTLE (71205-755-30)
- ndc11712057556060 TABLET in 1 BOTTLE (71205-755-60)
- ndc11712057559090 TABLET in 1 BOTTLE (71205-755-90)
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": "71205-755_22d9fd96-cad5-4762-9a56-0ff63357ed9e",
"productndc": "71205-755",
"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": "20220524",
"active_numerator_strength": "50"
}Related drugs
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