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Olmesartan Medoxomil

NDC 71205-458, Olmesartan Medoxomil, tablet, coated, from Proficient Rx LP.

Product NDC
71205-458
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206763
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-458 \
  -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
71205-458-307120504583030 TABLET, COATED in 1 BOTTLE (71205-458-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/eff8b514-bb7f-427e-a267-7dee25fff611

Use it

Look up 71205-458 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-458 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-458. 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.