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
- 71335-0398_812a5db0-ce5b-47df-a7f9-ca14cdb1532b
- Product NDC
- 71335-0398
- Form
- CAPSULE
- Composition / generic term
- Tamsulosin Hydrochloride
- Labeler
- Bryant Ranch Prepack
- 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
- 30 CAPSULE in 1 BOTTLE (71335-0398-1) · 71335-0398-1
- 100 CAPSULE in 1 BOTTLE (71335-0398-2) · 71335-0398-2
- 60 CAPSULE in 1 BOTTLE (71335-0398-3) · 71335-0398-3
- 10 CAPSULE in 1 BOTTLE (71335-0398-4) · 71335-0398-4
- 90 CAPSULE in 1 BOTTLE (71335-0398-5) · 71335-0398-5
- 180 CAPSULE in 1 BOTTLE (71335-0398-6) · 71335-0398-6
- 7 CAPSULE in 1 BOTTLE (71335-0398-7) · 71335-0398-7
- 15 CAPSULE in 1 BOTTLE (71335-0398-8) · 71335-0398-8
- 120 CAPSULE in 1 BOTTLE (71335-0398-9) · 71335-0398-9
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 →