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Alfuzosin Hydrochloride

NDC 47335-956, Alfuzosin Hydrochloride, tablet, extended release, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-956
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
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/47335-956 \
  -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
47335-956-0847335095608100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-08)
47335-956-18473350956181000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-18)
47335-956-814733509568190 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-81)
47335-956-834733509568330 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-83)
47335-956-8847335095688100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d2af616e-673a-4fdd-ace8-db2d0f154604

Use it

Look up 47335-956 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-956 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-956. 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.