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Moexipril Hydrochloride

NDC 0093-0017, Moexipril Hydrochloride, tablet, film coated, from Teva Pharmaceuticals USA, Inc..

Product NDC
0093-0017
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076204
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0093-0017 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MOEXIPRIL HYDROCHLORIDE7.5 mg/1

Pharmacologic classes

Angiotensin Converting Enzyme Inhibitor [EPC]; Angiotensin-converting Enzyme Inhibitors [MoA]

Package NDCNDC-11Package
0093-0017-0100093001701100 TABLET, FILM COATED in 1 BOTTLE (0093-0017-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5d4078f3-b621-475f-a4e6-005de2e62b32

  • NADAC price for package 00093001701

    GET /v1/drugs/nadac/00093001701

Use it

Look up 0093-0017 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0093-0017 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0093-0017. 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.