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Hydrochlorothiazide

NDC 71205-090, Hydrochlorothiazide, tablet, from Proficient Rx LP.

Product NDC
71205-090
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202556
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-090 \
  -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
71205-090-0071205009000100 TABLET in 1 BOTTLE (71205-090-00)
71205-090-03712050090033 TABLET in 1 BOTTLE (71205-090-03)
71205-090-07712050090077 TABLET in 1 BOTTLE (71205-090-07)
71205-090-107120500901010 TABLET in 1 BOTTLE (71205-090-10)
71205-090-307120500903030 TABLET in 1 BOTTLE (71205-090-30)
71205-090-607120500906060 TABLET in 1 BOTTLE (71205-090-60)
71205-090-907120500909090 TABLET in 1 BOTTLE (71205-090-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/48b4d633-ecfa-4748-80e8-6c0e3d8b067e

Use it

Look up 71205-090 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-090 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-090. 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.