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Spironolactone and Hydrochlorothiazide

NDC 66993-188, spironolactone and hydrochlorothiazide, tablet, film coated, from Prasco Laboratories.

Product NDC
66993-188
Status
Listed
Labeler
Prasco Laboratories
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA012616
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/66993-188 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SPIRONOLACTONE25 mg/1
  • HYDROCHLOROTHIAZIDE25 mg/1

Pharmacologic classes

Aldosterone Antagonist [EPC]; Aldosterone Antagonists [MoA]; Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]

Package NDCNDC-11Package
66993-188-0266993018802100 TABLET, FILM COATED in 1 BOTTLE (66993-188-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9d350fa2-d568-4970-a7a5-d128ff5d0a2f

  • NADAC price for package 66993018802

    GET /v1/drugs/nadac/66993018802

Use it

Look up 66993-188 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/66993-188 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 66993-188. 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.