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OLMESARTAN MEDOXOMIL

NDC 31722-852, OLMESARTAN MEDOXOMIL, tablet, film coated, from Camber Pharmaceuticals, Inc..

Product NDC
31722-852
Status
Listed
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205499
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-852 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLMESARTAN MEDOXOMIL5 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]

Package NDCNDC-11Package
31722-852-303172208523030 TABLET, FILM COATED in 1 BOTTLE (31722-852-30)
31722-852-903172208529090 TABLET, FILM COATED in 1 BOTTLE (31722-852-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/53b8d406-a4f3-46ee-9aec-d70f7d806876

  • NADAC price for package 31722085230

    GET /v1/drugs/nadac/31722085230

  • NADAC price for package 31722085290

    GET /v1/drugs/nadac/31722085290

Use it

Look up 31722-852 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-852 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-852. 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.