Active Ingredient: TAMOXIFEN CITRATE
Proprietary Name: TAMOXIFEN CITRATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 10MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A206694
Product Number: 001
Approval Date: Oct 27, 2017
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information