Active Ingredient: ANAGRELIDE HYDROCHLORIDE
Proprietary Name: ANAGRELIDE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 0.5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A076468
Product Number: 001
Approval Date: Apr 18, 2005
Applicant Holder Full Name: IVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA
Marketing Status:
Prescription
Patent and Exclusivity Information