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Olmesartan Medoxomil

NDC 71335-2362, Olmesartan Medoxomil, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
71335-2362
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204798
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2362 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLMESARTAN MEDOXOMIL40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71335-2362-17133523620130 TABLET, FILM COATED in 1 BOTTLE (71335-2362-1)
71335-2362-27133523620290 TABLET, FILM COATED in 1 BOTTLE (71335-2362-2)
71335-2362-37133523620328 TABLET, FILM COATED in 1 BOTTLE (71335-2362-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0a49d951-dd1b-413b-99e5-d3119267c46c

Use it

Look up 71335-2362 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2362 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2362. 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.