FDA's Approved Drug Products database

Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient SIMVASTATIN
Proprietary Name SIMVASTATIN
Applicant SUN PHARM INDS LTD
Dosage Form;Route ORAL
Strength 80MG
Application Type A
Product Number 5
Approval Date 2006/06/23
RX/OTC/DISCN No
Applicant Full Name DISCN
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