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HYDROCHLOROTHIAZIDE

NDC 42708-164, hydrochlorothiazide, tablet, from QPharma Inc.

Product NDC
42708-164
Status
Listed
Labeler
QPharma Inc
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA085182
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42708-164 \
  -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
42708-164-304270801643030 TABLET in 1 BOTTLE, PLASTIC (42708-164-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f795db5e-d5ef-4a20-e053-6394a90a7fda

Use it

Look up 42708-164 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42708-164 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42708-164. 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.