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:
Application Number: A077613
Product Number: 001
Approval Date: Jun 27, 2006
Applicant Holder Full Name: RISING PHARMA HOLDINGS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information