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Spironolactone and Hydrochlorothiazide

NDC 71335-2202, Spironolactone and Hydrochlorothiazide, tablet, from Bryant Ranch Prepack.

Product NDC
71335-2202
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA089534
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2202 \
  -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
71335-2202-171335220201100 TABLET in 1 BOTTLE, PLASTIC (71335-2202-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c5258ea3-3aac-48fd-be5a-f8e4a47ca94a

Use it

Look up 71335-2202 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2202 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2202. 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.