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Hydrochlorothiazide

NDC 71205-751, Hydrochlorothiazide, tablet, from Proficient Rx LP.

Product NDC
71205-751
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA083177
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-751 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCHLOROTHIAZIDE50 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71205-751-307120507513030 TABLET in 1 BOTTLE (71205-751-30)
71205-751-607120507516060 TABLET in 1 BOTTLE (71205-751-60)
71205-751-907120507519090 TABLET in 1 BOTTLE (71205-751-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c4fe84e3-c291-4220-95c1-a2bd02b1e134

Use it

Look up 71205-751 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-751 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-751. 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.