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Hydrochlorothiazide

NDC 72789-381, Hydrochlorothiazide, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-381
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA087059
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72789-381 \
  -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
72789-381-907278903819090 TABLET in 1 BOTTLE, PLASTIC (72789-381-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1dc47186-3ecf-456f-b6d6-ba0f75c2504b

Use it

Look up 72789-381 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-381 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-381. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.