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Moexipril Hydrochloride

NDC 62135-967, Moexipril Hydrochloride, tablet, film coated, from Chartwell RX, LLC.

Product NDC
62135-967
Status
Listed
Labeler
Chartwell RX, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077536
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62135-967 \
  -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
62135-967-906213509679090 TABLET, FILM COATED in 1 BOTTLE (62135-967-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5c24072c-9769-4cb5-b8da-bf814d21391d

  • NADAC price for package 62135096790

    GET /v1/drugs/nadac/62135096790

Use it

Look up 62135-967 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62135-967 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62135-967. 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.