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Hydrochlorothiazide

NDC 43063-747, Hydrochlorothiazide, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
43063-747
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
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/43063-747 \
  -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
43063-747-0143063074701100 TABLET in 1 BOTTLE, PLASTIC (43063-747-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/27a7e751-8aca-440e-95e4-cfecae1a2465

Use it

Look up 43063-747 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43063-747 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43063-747. 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.