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
- 62756-160_52595417-3e2e-4d58-9167-dd5b2bf1b082
- Product NDC
- 62756-160
- Form
- CAPSULE
- Composition / generic term
- Tamsulosin Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100715
- 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 (62756-160-08) · 62756-160-08
- 500 CAPSULE in 1 BOTTLE (62756-160-13) · 62756-160-13
- 1000 CAPSULE in 1 BOTTLE (62756-160-18) · 62756-160-18
- 90 CAPSULE in 1 BOTTLE (62756-160-81) · 62756-160-81
- 30 CAPSULE in 1 BOTTLE (62756-160-83) · 62756-160-83
- 100 CAPSULE in 1 BOTTLE (62756-160-88) · 62756-160-88
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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