NDC 68382-132

Tamsulosin Hydrochloride 0.4 mg capsule

On the label: Zydus Pharmaceuticals (USA) Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action

Product details

Generic drug
Tamsulosin: every company that makes it
Form
capsule, oral
Strength
0.4 mg
Approval
ANDA ANDA078225
On the market since
Apr 27, 2010
Package NDCs
68382-132-01 68382-132-05 68382-132-06 68382-132-10 68382-132-14 68382-132-16 68382-132-30 68382-132-77
Official label
DailyMed (National Library of Medicine), updated Nov 8, 2023

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