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Benazepril Hydrochloride

NDC 68788-8877, Benazepril Hydrochloride, tablet, film coated, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8877
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078212
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8877 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BENAZEPRIL HYDROCHLORIDE10 mg/1

Pharmacologic classes

Angiotensin Converting Enzyme Inhibitor [EPC]; Angiotensin-converting Enzyme Inhibitors [MoA]; Decreased Blood Pressure [PE]

Package NDCNDC-11Package
68788-8877-168788887701100 TABLET, FILM COATED in 1 BOTTLE (68788-8877-1)
68788-8877-36878888770330 TABLET, FILM COATED in 1 BOTTLE (68788-8877-3)
68788-8877-66878888770660 TABLET, FILM COATED in 1 BOTTLE (68788-8877-6)
68788-8877-96878888770990 TABLET, FILM COATED in 1 BOTTLE (68788-8877-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/91a3d0f7-d2df-4230-ad9e-b32f7312d337

Use it

Look up 68788-8877 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8877 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8877. 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.