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HYDROCHLOROTHIAZIDE

NDC 71335-9647, HYDROCHLOROTHIAZIDE, tablet, from Bryant Ranch Prepack.

Product NDC
71335-9647
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040702
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-9647 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCHLOROTHIAZIDE12.5 mg/1

Pharmacologic classes

Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]

Package NDCNDC-11Package
71335-9647-17133596470130 TABLET in 1 BOTTLE, PLASTIC (71335-9647-1)
71335-9647-27133596470290 TABLET in 1 BOTTLE, PLASTIC (71335-9647-2)
71335-9647-37133596470314 TABLET in 1 BOTTLE, PLASTIC (71335-9647-3)
71335-9647-471335964704100 TABLET in 1 BOTTLE, PLASTIC (71335-9647-4)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/03b7e52e-0003-47c3-af12-93ef00800b37

Use it

Look up 71335-9647 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-9647 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-9647. 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.