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PACK IN HAND · ONE-PAGE CHECK

Medicine pack check sheet

Print this sheet or fill it in before speaking with a pharmacist or clinician. Copy only what is printed on the pack in hand. The published fields below are starting points from this record, not proof that your pack is the same product.

Published record starting point

Record display name
UROXATRAL
Generic name / active ingredient
alfuzosin hydrochloride extended-release tablets
Dosage-form class
Alfuzosin hydrochloride 10 mg oral extended-release tablet: a round three-layer tablet with one white layer between two yellow layers, debossed X10. The current label says to swallow it whole and not crush, split or chew it.
Route
Oral
Record reviewed
2026-09-02

Copy from the pack in hand

Source-linked reading points

  • This is a three-layer extended-release tablet. Do not split, crush or chew it because of swallowing difficulty, a desired reduction or its layered appearance; have a pharmacist review the actual pack and current label for handling or another suitable form.
  • The label warns about postural hypotension, dizziness and syncope and notes potentially increased risk with antihypertensive medicines or nitrates. Older adults, people with falls or several cardiovascular medicines should prioritise full-list, blood-pressure and exact-pack review with a clinician or pharmacist; do not self-separate or stop a pack.
  • The label contraindicates potent CYP3A4 inhibitors such as ketoconazole, itraconazole and ritonavir and warns that PDE5 inhibitors such as sildenafil or tadalafil can increase symptomatic-hypotension risk. The site provides no self-directed spacing, halving or temporary-stop plan.
  • Before cataract surgery or another eye procedure, tell the eye team about current or previous UROXATRAL/other alpha-blocker use. The label does not support self-stopping for this reason.

Reviewed presentation examples — compare every field

  • Alfuzosin hydrochloride 10 mg per tablet; 30-tablet child-resistant bottleNDC 59212-200-30
  • Alfuzosin hydrochloride 10 mg per tablet; 100-tablet child-resistant bottleNDC 59212-200-10

EDITORIAL RECORD

Who prepared and checked this page

Byline
OriginDrug Content Editorial
Review role
Public primary-source verification
Last reviewed
2026-09-02
Source record
3 clickable primary-source entry points are listed with this dossier.

The review role checks source traceability, stated market, document version and product-identity fields. It is not a claim of clinical licensure, prescribing authority or individual pharmacy service. Read the editorial policy.

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