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Hydrochlorothiazide

NDC 71205-419, Hydrochlorothiazide, tablet, from Proficient Rx LP.

Product NDC
71205-419
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040907
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-419 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCHLOROTHIAZIDE25 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71205-419-147120504191414 TABLET in 1 BOTTLE (71205-419-14)
71205-419-307120504193030 TABLET in 1 BOTTLE (71205-419-30)
71205-419-607120504196060 TABLET in 1 BOTTLE (71205-419-60)
71205-419-907120504199090 TABLET in 1 BOTTLE (71205-419-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ff448eb4-b48f-46f5-ac30-f03aad08f9f5

Use it

Look up 71205-419 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-419 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-419. 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.