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
- 65841-695_b05d1829-8334-4145-b49d-6074624bc499
- Product NDC
- 65841-695
- Form
- CAPSULE
- Composition / generic term
- Tamsulosin Hydrochloride
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100427
- 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 (65841-695-01) · 65841-695-01
- 500 CAPSULE in 1 BOTTLE (65841-695-05) · 65841-695-05
- 30 CAPSULE in 1 BOTTLE (65841-695-06) · 65841-695-06
- 1000 CAPSULE in 1 BOTTLE (65841-695-10) · 65841-695-10
- 60 CAPSULE in 1 BOTTLE (65841-695-14) · 65841-695-14
- 90 CAPSULE in 1 BOTTLE (65841-695-16) · 65841-695-16
- 10 BLISTER PACK in 1 CARTON (65841-695-77) / 10 CAPSULE in 1 BLISTER PACK · 65841-695-77
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 →