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Spironolactone

NDC 76420-062, spironolactone, tablet, film coated, from Asclemed USA, Inc..

Product NDC
76420-062
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203512
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-062 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SPIRONOLACTONE25 mg/1

Pharmacologic classes

Aldosterone Antagonist [EPC]; Aldosterone Antagonists [MoA]

Package NDCNDC-11Package
76420-062-0176420006201100 TABLET, FILM COATED in 1 BOTTLE (76420-062-01)
76420-062-307642000623030 TABLET, FILM COATED in 1 BOTTLE (76420-062-30)
76420-062-607642000626060 TABLET, FILM COATED in 1 BOTTLE (76420-062-60)
76420-062-907642000629090 TABLET, FILM COATED in 1 BOTTLE (76420-062-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/31c42b3e-f076-49d9-aa61-6cef0dbb5543

Use it

Look up 76420-062 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-062 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-062. 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.