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Prednisolone Sodium Phosphate

NDC 17856-8815, Prednisolone Sodium Phosphate, solution, from Atlantic Biologicals Corp.

Product NDC
17856-8815
Status
Listed
Labeler
Atlantic Biologicals Corp
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203559
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17856-8815 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISOLONE SODIUM PHOSPHATE15 mg/5mL

Pharmacologic classes

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

Package NDCNDC-11Package
17856-8815-11785688150150 CUP, UNIT-DOSE in 1 CASE (17856-8815-1) / 5 mL in 1 CUP, UNIT-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/401f7ba6-a4a2-9ae6-e063-6394a90a4210

Use it

Look up 17856-8815 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17856-8815 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17856-8815. 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.