United States · FDA National Drug Code directory

Tamsulosin Hydrochloride

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
65862-598_94771a21-3051-46cc-8deb-200bc9f3dcb3
Product NDC
65862-598
Form
CAPSULE
Composition / generic term
Tamsulosin Hydrochloride
Labeler
Aurobindo Pharma Limited
Marketing category
ANDA
Marketing start / end (source format)
20130430
Source listing expiry
20261231

Source-listed ingredients

  • TAMSULOSIN HYDROCHLORIDE — .4 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE in 1 BOTTLE (65862-598-01) · 65862-598-01
  • 500 CAPSULE in 1 BOTTLE (65862-598-05) · 65862-598-05
  • 3 BLISTER PACK in 1 CARTON (65862-598-10) / 10 CAPSULE in 1 BLISTER PACK · 65862-598-10

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →
Tamsulosin Hydrochloride — United States | Molindra Medicines