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Lisinopril and Hydrochlorothiazide

NDC 68071-2303, Lisinopril and Hydrochlorothiazide Tablets, tablet, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-2303
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204058
DEA schedule
None
Request
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Product

Active ingredients and packages

Active ingredients

  • LISINOPRIL20 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
68071-2303-36807123030330 TABLET in 1 BOTTLE (68071-2303-3)
68071-2303-868071230308180 TABLET in 1 BOTTLE (68071-2303-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b4c9abf7-a2c6-7042-e053-2a95a90a7653

Use it

Look up 68071-2303 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2303 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-2303. 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.