Active Ingredient: TAMOXIFEN CITRATE
Proprietary Name: TAMOXIFEN CITRATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 20MG BASE
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A075797
Product Number: 002
Approval Date: Feb 20, 2003
Applicant Holder Full Name: DR REDDYS LABORATORIES SA
Marketing Status:
Prescription
Patent and Exclusivity Information
