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Serving 500+ biopharmaceutical companies globally:

Federal Trade Commission
Express Scripts
Boehringer Ingelheim
Johnson and Johnson
Harvard Business School
Farmers Insurance

Generated: September 21, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 202433

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NDA 202433 describes TAMSULOSIN HYDROCHLORIDE, which is a drug marketed by Synthon Pharms, Alkem Labs Ltd, Mylan, Anchen Pharms, Sandoz, Zydus Pharms Usa Inc, Teva Pharms, Sun Pharm Inds Ltd, Aurobindo Pharma Ltd, Wockhardt, Macleods Pharms Ltd, and Impax Labs, and is included in twelve NDAs. It is available from fifty-one suppliers. Additional details are available on the TAMSULOSIN HYDROCHLORIDE profile page.

The generic ingredient in TAMSULOSIN HYDROCHLORIDE is tamsulosin hydrochloride. There are thirty-two drug master file entries for this compound. Fifty-three suppliers are listed for this compound. Additional details are available on the tamsulosin hydrochloride profile page.

Summary for NDA: 202433

Therapeutic Class:Genitourinary Agents
Formulation / Manufacturing:see details

Pharmacology for NDA: 202433

Mechanism of ActionAdrenergic alpha-Antagonists

Suppliers and Packaging for NDA: 202433

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
tamsulosin hydrochloride
CAPSULE;ORAL 202433 ANDA NCS HealthCare of KY, Inc dba Vangard Labs 0615-8055 0615-8055-05 15 CAPSULE in 1 BLISTER PACK (0615-8055-05)
tamsulosin hydrochloride
CAPSULE;ORAL 202433 ANDA NCS HealthCare of KY, Inc dba Vangard Labs 0615-8055 0615-8055-39 30 CAPSULE in 1 BLISTER PACK (0615-8055-39)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:CAPSULE;ORALStrength0.4MG
Approval Date:Apr 30, 2013TE:ABRLD:No

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Serving 500+ biopharmaceutical companies globally:

Daiichi Sankyo
US Army
Boehringer Ingelheim
Federal Trade Commission

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