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SPIRONOLACTONE

NDC 17856-1233, spironolactone, suspension, from Atlantic Biologicals Corp..

Product NDC
17856-1233
Status
Listed
Labeler
Atlantic Biologicals Corp.
Dosage form
SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA209478
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17856-1233 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SPIRONOLACTONE25 mg/5mL

Pharmacologic classes

Aldosterone Antagonist [EPC]; Aldosterone Antagonists [MoA]

Package NDCNDC-11Package
17856-1233-117856123301110 SYRINGE in 1 CASE (17856-1233-1) / 1 mL in 1 SYRINGE
17856-1233-21785612330245 SYRINGE in 1 CASE (17856-1233-2) / 2.5 mL in 1 SYRINGE
17856-1233-317856123303110 SYRINGE in 1 CASE (17856-1233-3) / 3 mL in 1 SYRINGE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5a203ae4-0ed1-0099-e063-6294a90abc85

Use it

Look up 17856-1233 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17856-1233 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17856-1233. 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.