United States · FDA National Drug Code directory

Dutasteride and 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: 68382-640_9e44a416-1d3d-418c-a113-f6c65175b564
Product NDC: 68382-640
Form: CAPSULE
Composition / generic term: Dutasteride and tamsulosin hydrochloride
Labeler: Zydus Pharmaceuticals USA Inc.
Marketing category: ANDA
Marketing start / end (source format): 20180604
Source listing expiry: 20261231

Source-listed ingredients

DUTASTERIDE — .5 mg/1
TAMSULOSIN HYDROCHLORIDE — .4 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 CAPSULE in 1 BOTTLE (68382-640-06) · 68382-640-06
90 CAPSULE in 1 BOTTLE (68382-640-16) · 68382-640-16

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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