NDC 71610-835 – Tamsulosin Hydrochloride

Tamsulosin Hydrochloride .4 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71610-835

Product details

Brand name
Tamsulosin Hydrochloride
Generic name
Tamsulosin Hydrochloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA202433
Marketed since
April 30, 2013
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Tamsulosin Hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
71610-835-3030 CAPSULE in 1 BOTTLE (71610-835-30)May 24, 2024
71610-835-5360 CAPSULE in 1 BOTTLE (71610-835-53)May 24, 2024
71610-835-6090 CAPSULE in 1 BOTTLE (71610-835-60)May 24, 2024
71610-835-80180 CAPSULE in 1 BOTTLE (71610-835-80)May 24, 2024

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