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Irbesartan and Hydrochlorothiazide

NDC 72162-1035, Irbesartan and Hydrochlorothiazide, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
72162-1035
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077369
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1035 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IRBESARTAN150 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
72162-1035-97216210350990 TABLET, FILM COATED in 1 BOTTLE (72162-1035-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5029c9f7-6233-4a6f-ace9-2268cc8e286d

Use it

Look up 72162-1035 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1035 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-1035. 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.