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United States · US · US:50090-0559_54821cc4-1238-4ab7-926f-4e6a185d55e5
Prednisolone Acetate
Orange BookUNIISPLATC S02BA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeS02BA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1150090055901 BOTTLE, PLASTIC in 1 CARTON (50090-0559-0) / 10 mL in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
8B2807733D
PREDNISOLONE ACETATE
RxCUI 34372
Orange Book
N017469
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "8B2807733D",
"rxcui": "34372",
"inchikey": "LRJOMUJRLNCICJ-JZYPGELDSA-N",
"display_name": "PREDNISOLONE ACETATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "OPHTHALMIC",
"spl_meta": {
"02fc6f0b-d053-49e1-82de-f272dd05d529": {
"match": "brand_token",
"title": "PREDNISOLONE ACETATE SUSPENSION/ DROPS [SPORTPHARM LLC]",
"spl_version": "2",
"published_date": "2026-04-27"
}
},
"productid": "50090-0559_54821cc4-1238-4ab7-926f-4e6a185d55e5",
"productndc": "50090-0559",
"dosage_form": "SUSPENSION/ DROPS",
"orange_book": {
"appl_no": "017469",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "1%",
"product_no": "001",
"approval_date": "Approved Prior to Jan 1, 1982"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PREDNISOLONE ACETATE",
"proprietary_name": "Prednisolone Acetate",
"active_ingred_unit": "mg/mL",
"application_number": "NDA017469",
"marketing_category": "NDA AUTHORIZED GENERIC",
"nonproprietary_name": "Prednisolone Acetate",
"start_marketing_date": "19941215",
"active_numerator_strength": "10"
}Related drugs
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