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Hydrochlorothiazide

NDC 0172-2089, Hydrochlorothiazide, tablet, from Teva Pharmaceuticals USA, Inc..

Product NDC
0172-2089
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
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/0172-2089 \
  -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
0172-2089-6000172208960100 TABLET in 1 BOTTLE (0172-2089-60)
0172-2089-80001722089801000 TABLET in 1 BOTTLE (0172-2089-80)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e2270db4-2930-4ec5-ac96-2b4542aed367

  • NADAC price for package 00172208960

    GET /v1/drugs/nadac/00172208960

  • NADAC price for package 00172208980

    GET /v1/drugs/nadac/00172208980

Use it

Look up 0172-2089 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0172-2089 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0172-2089. 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.