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
- 61919-703_500f0251-b6c2-8ff8-e063-6394a90a8574
- Product NDC
- 61919-703
- Form
- CAPSULE
- Composition / generic term
- TAMSULOSIN HYDROCHLORIDE
- Labeler
- DIRECT RX
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181109
- Source listing expiry
- 20271231
Source-listed ingredients
- TAMSULOSIN HYDROCHLORIDE — .4 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 CAPSULE in 1 CAPSULE (61919-703-90) · 61919-703-90
Source and coverage
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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.
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