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OLMESARTAN MEDOXOMIL

NDC 31722-853, OLMESARTAN MEDOXOMIL, tablet, film coated, from Camber Pharmaceuticals, Inc..

Product NDC
31722-853
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/31722-853 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLMESARTAN MEDOXOMIL20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
31722-853-303172208533030 TABLET, FILM COATED in 1 BOTTLE (31722-853-30)
31722-853-903172208539090 TABLET, FILM COATED in 1 BOTTLE (31722-853-90)

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 31722085330

    GET /v1/drugs/nadac/31722085330

  • NADAC price for package 31722085390

    GET /v1/drugs/nadac/31722085390

Use it

Look up 31722-853 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-853 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-853. 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.