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Spironolactone

NDC 43063-835, spironolactone, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..

Product NDC
43063-835
Status
Listed
Labeler
PD-Rx Pharmaceuticals, 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/43063-835 \
  -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
43063-835-304306308353030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-835-30)
43063-835-904306308359090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-835-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c0efa529-2870-4260-b604-2f30e2cbb87b

Use it

Look up 43063-835 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43063-835 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43063-835. 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.