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Enalapril Maleate

NDC 68682-712, Enalapril Maleate, tablet, from OCEANSIDE PHARMACEUTICALS.

Product NDC
68682-712
Status
Listed
Labeler
OCEANSIDE PHARMACEUTICALS
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA018998
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68682-712 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ENALAPRIL MALEATE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68682-712-0168682071201100 TABLET in 1 BOTTLE (68682-712-01)
68682-712-10686820712101000 TABLET in 1 BOTTLE (68682-712-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ebd2a62d-a704-4f8a-a104-749a5296502f

Use it

Look up 68682-712 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68682-712 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68682-712. 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.