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OLMESARTAN MEDOXOMIL

NDC 72189-137, OLMESARTAN MEDOXOMIL, tablet, film coated, from direct rx.

Product NDC
72189-137
Status
Listed
Labeler
direct rx
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207662
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72189-137 \
  -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
72189-137-307218901373030 TABLET, FILM COATED in 1 BOTTLE (72189-137-30)
72189-137-907218901379090 TABLET, FILM COATED in 1 BOTTLE (72189-137-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b57e47a5-43e0-d1c5-e053-2a95a90a2b07

Use it

Look up 72189-137 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-137 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-137. 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.