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Lisinopril and Hydrochlorothiazide

NDC 42708-150, Lisinopril and Hydrochlorothiazide, tablet, from QPharma, Inc..

Product NDC
42708-150
Status
Listed
Labeler
QPharma, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077912
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42708-150 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCHLOROTHIAZIDE12.5 mg/1
  • LISINOPRIL10 mg/1

Pharmacologic classes

Angiotensin Converting Enzyme Inhibitor [EPC]; Angiotensin-converting Enzyme Inhibitors [MoA]; Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]

Package NDCNDC-11Package
42708-150-304270801503030 TABLET in 1 BOTTLE, PLASTIC (42708-150-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c80b2164-3795-6668-e053-2a95a90a4d45

Use it

Look up 42708-150 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42708-150 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42708-150. 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.