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Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient SILDENAFIL CITRATE
Proprietary Name SILDENAFIL CITRATE
Applicant WATSON LABS INC
Dosage Form;Route ORAL
Strength EQ 20MG BASE
Application Type A
Product Number 1
Approval Date 2012/11/06
RX/OTC/DISCN No
Applicant Full Name RX
TE Code AB
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