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United States · US · US:71205-089_f37da7b3-fa10-473c-acab-371529fee8c9
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 · 17
- ndc117120508900100 TABLET in 1 BOTTLE (71205-089-00)
- ndc1171205089055 TABLET in 1 BOTTLE (71205-089-05)
- ndc1171205089066 TABLET in 1 BOTTLE (71205-089-06)
- ndc1171205089077 TABLET in 1 BOTTLE (71205-089-07)
- ndc1171205089088 TABLET in 1 BOTTLE (71205-089-08)
- ndc11712050891010 TABLET in 1 BOTTLE (71205-089-10)
- ndc11712050891212 TABLET in 1 BOTTLE (71205-089-12)
- ndc11712050891515 TABLET in 1 BOTTLE (71205-089-15)
- ndc11712050891818 TABLET in 1 BOTTLE (71205-089-18)
- ndc11712050892020 TABLET in 1 BOTTLE (71205-089-20)
- ndc11712050892121 TABLET in 1 BOTTLE (71205-089-21)
- ndc11712050892424 TABLET in 1 BOTTLE (71205-089-24)
- ndc11712050892727 TABLET in 1 BOTTLE (71205-089-27)
- ndc11712050893030 TABLET in 1 BOTTLE (71205-089-30)
- ndc11712050893636 TABLET in 1 BOTTLE (71205-089-36)
- ndc11712050894040 TABLET in 1 BOTTLE (71205-089-40)
- ndc11712050894242 TABLET in 1 BOTTLE (71205-089-42)
Annotations
UNII (FDA Substance ID)
VB0R961HZT
PREDNISONE
RxCUI 8640
Orange Book
A040611
AB
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": "71205-089_f37da7b3-fa10-473c-acab-371529fee8c9",
"productndc": "71205-089",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "040611",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "1MG",
"product_no": "001",
"approval_date": "Jun 6, 2005"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PREDNISONE",
"proprietary_name": "Prednisone",
"active_ingred_unit": "mg/1",
"application_number": "ANDA040611",
"marketing_category": "ANDA",
"nonproprietary_name": "Prednisone",
"start_marketing_date": "20050606",
"active_numerator_strength": "1"
}Related drugs
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