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Alfuzosin Hydrochloride

NDC 71335-2146, Alfuzosin Hydrochloride, tablet, extended release, from Bryant Ranch Prepack.

Product NDC
71335-2146
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/71335-2146 \
  -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
71335-2146-17133521460130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-1)
71335-2146-27133521460260 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-2)
71335-2146-37133521460390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-3)
71335-2146-471335214604120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-4)
71335-2146-571335214605100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/98fa10c2-7c12-44aa-9112-e2fd6fa71d06

Use it

Look up 71335-2146 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2146 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2146. 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.