Active Ingredient: SILDENAFIL CITRATE
Proprietary Name: SILDENAFIL CITRATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 20MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A204883
Product Number: 001
Approval Date: Jun 20, 2016
Applicant Holder Full Name: RUBICON RESEARCH PRIVATE LTD
Marketing Status:
Prescription
Patent and Exclusivity Information