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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

  • ndc11
    5009005590
    1 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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