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QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE

NDC 65862-163, QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-163
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078450
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-163 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • QUINAPRIL HYDROCHLORIDE20 mg/1
  • HYDROCHLOROTHIAZIDE25 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
65862-163-906586201639090 TABLET, FILM COATED in 1 BOTTLE (65862-163-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/50a58159-9572-4445-9859-b392632597da

Use it

Look up 65862-163 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-163 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-163. 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.