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Alfuzosin Hydrochloride

NDC 72162-1449, Alfuzosin Hydrochloride, tablet, extended release, from Bryant Ranch Prepack.

Product NDC
72162-1449
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA079057
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1449 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALFUZOSIN HYDROCHLORIDE10 mg/1

Pharmacologic classes

Adrenergic alpha-Antagonists [MoA]; alpha-Adrenergic Blocker [EPC]

Package NDCNDC-11Package
72162-1449-97216214490990 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1449-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3a541efa-9eed-4a27-b602-7999fc6f59aa

Use it

Look up 72162-1449 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1449 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-1449. 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.