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Spironolactone

NDC 70518-3655, Spironolactone, tablet, coated, from REMEDYREPACK INC..

Product NDC
70518-3655
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040750
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3655 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SPIRONOLACTONE50 mg/1

Pharmacologic classes

Aldosterone Antagonist [EPC]; Aldosterone Antagonists [MoA]

Package NDCNDC-11Package
70518-3655-27051836550230 TABLET, COATED in 1 BLISTER PACK (70518-3655-2)
70518-3655-370518365503100 POUCH in 1 BOX (70518-3655-3) / 1 TABLET, COATED in 1 POUCH (70518-3655-4)
70518-3655-57051836550530 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3655-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b119ed8a-289a-46c5-9778-6b07e4c061c4

Use it

Look up 70518-3655 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3655 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3655. 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.