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Hydrochlorothiazide

NDC 72789-512, Hydrochlorothiazide, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-512
Status
Listed
Labeler
PD-Rx Pharmaceuticals, 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/72789-512 \
  -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
72789-512-307278905123030 TABLET in 1 BOTTLE, PLASTIC (72789-512-30)
72789-512-607278905126060 TABLET in 1 BOTTLE, PLASTIC (72789-512-60)
72789-512-907278905129090 TABLET in 1 BOTTLE, PLASTIC (72789-512-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c182b6a9-1a31-45ee-9cea-a557c99f5db7

Use it

Look up 72789-512 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-512 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-512. 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.