alfuzosin hydrochloride

Generic: alfuzosin hydrochloride

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alfuzosin hydrochloride
Generic Name alfuzosin hydrochloride
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

alfuzosin hydrochloride 10 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 47335-956
Product ID 47335-956_70258299-7c72-4a10-8d0c-4a5e3b2a0fc8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079057
Listing Expiration 2026-12-31
Marketing Start 2011-11-22

Pharmacologic Class

Classes
adrenergic alpha-antagonists [moa] alpha-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 47335956
Hyphenated Format 47335-956

Supplemental Identifiers

RxCUI
861132
UPC
0347335956818
UNII
75046A1XTN

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name alfuzosin hydrochloride (source: ndc)
Generic Name alfuzosin hydrochloride (source: ndc)
Application Number ANDA079057 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-08)
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-18)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-81)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-83)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-88)
source: ndc

Packages (5)

47335-956-08 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-08) 47335-956-18 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-18) 47335-956-81 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-81) 47335-956-83 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-83) 47335-956-88 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-88)

Ingredients (1)

alfuzosin hydrochloride (10 mg/1)

Linked Drug Pages (1)

Alfuzosin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "70258299-7c72-4a10-8d0c-4a5e3b2a0fc8", "openfda": {"upc": ["0347335956818"], "unii": ["75046A1XTN"], "rxcui": ["861132"], "spl_set_id": ["d2af616e-673a-4fdd-ace8-db2d0f154604"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-08)", "package_ndc": "47335-956-08", "marketing_start_date": "20111122"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-18)", "package_ndc": "47335-956-18", "marketing_start_date": "20111122"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-81)", "package_ndc": "47335-956-81", "marketing_start_date": "20111122"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-83)", "package_ndc": "47335-956-83", "marketing_start_date": "20111122"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-88)", "package_ndc": "47335-956-88", "marketing_start_date": "20111122"}], "brand_name": "Alfuzosin Hydrochloride", "product_id": "47335-956_70258299-7c72-4a10-8d0c-4a5e3b2a0fc8", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "47335-956", "generic_name": "Alfuzosin Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alfuzosin Hydrochloride", "active_ingredients": [{"name": "ALFUZOSIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA079057", "marketing_category": "ANDA", "marketing_start_date": "20111122", "listing_expiration_date": "20261231"}