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Olmesartan Medoxomil and Hydrochlorothiazide

NDC 71335-0845, Olmesartan Medoxomil and Hydrochlorothiazide, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
71335-0845
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205391
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0845 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLMESARTAN MEDOXOMIL40 mg/1
  • HYDROCHLOROTHIAZIDE12.5 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]; Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]

Package NDCNDC-11Package
71335-0845-17133508450130 TABLET, FILM COATED in 1 BOTTLE (71335-0845-1)
71335-0845-27133508450290 TABLET, FILM COATED in 1 BOTTLE (71335-0845-2)
71335-0845-37133508450328 TABLET, FILM COATED in 1 BOTTLE (71335-0845-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0360db3a-17cf-4d24-97ba-e0a6fcc94351

Use it

Look up 71335-0845 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0845 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-0845. 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.