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PredniSONE

NDC 17856-3722, PredniSONE, solution, from Atlantic Biologicals Corps.

Product NDC
17856-3722
Status
Listed
Labeler
Atlantic Biologicals Corps
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA088703
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17856-3722 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISONE5 mg/5mL

Pharmacologic classes

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

Package NDCNDC-11Package
17856-3722-1178563722015 mL in 1 CUP (17856-3722-1)
17856-3722-21785637220245 SYRINGE in 1 CASE (17856-3722-2) / 5 mL in 1 SYRINGE
17856-3722-31785637220345 SYRINGE in 1 CASE (17856-3722-3) / 5 mL in 1 SYRINGE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/07be390e-ef1e-4bf9-a9da-4338b5f6cfa5

Use it

Look up 17856-3722 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17856-3722 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17856-3722. 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.