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OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE

NDC 67877-452, OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE, tablet, film coated, from Ascend Laboratories, LLC.

Product NDC
67877-452
Status
Listed
Labeler
Ascend Laboratories, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207037
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67877-452 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLMESARTAN MEDOXOMIL40 mg/1
  • HYDROCHLOROTHIAZIDE12.5 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]; Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]

Package NDCNDC-11Package
67877-452-306787704523030 TABLET, FILM COATED in 1 BOTTLE (67877-452-30)
67877-452-906787704529090 TABLET, FILM COATED in 1 BOTTLE (67877-452-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/798fee33-51ad-45d0-82f3-09289304139f

  • NADAC price for package 67877045230

    GET /v1/drugs/nadac/67877045230

  • NADAC price for package 67877045290

    GET /v1/drugs/nadac/67877045290

Use it

Look up 67877-452 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67877-452 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67877-452. 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.