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SPIRONOLACTONE

NDC 71335-2203, SPIRONOLACTONE, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
71335-2203
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA089424
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2203 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SPIRONOLACTONE100 mg/1

Pharmacologic classes

Aldosterone Antagonist [EPC]; Aldosterone Antagonists [MoA]

Package NDCNDC-11Package
71335-2203-171335220301500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2203-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bb1423e8-1517-44c5-98e0-99be24ce269b

Use it

Look up 71335-2203 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2203 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2203. 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.