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Prednisolone Sodium Phosphate

NDC 13925-166, Prednisolone Sodium Phosphate, solution, from Seton Pharmaceuticals, LLC.

Product NDC
13925-166
Status
Listed
Labeler
Seton Pharmaceuticals, LLC
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA019157
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/13925-166 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISOLONE SODIUM PHOSPHATE5 mg/5mL

Pharmacologic classes

Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]

Package NDCNDC-11Package
13925-166-0413925016604120 mL in 1 BOTTLE (13925-166-04)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/833ba492-8823-43b4-9a91-8b28d94a740b

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=13925-166

Use it

Look up 13925-166 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/13925-166 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 13925-166. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.