Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 076530

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ANAGRELIDE HYDROCHLORIDE (ANAGRELIDE HYDROCHLORIDE)
EQ 0.5MG BASE
Marketing Status: Discontinued

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: A076530
Product Number: 001
Approval Date: Apr 18, 2005
Applicant Holder Full Name: BARR LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

ANAGRELIDE HYDROCHLORIDE (ANAGRELIDE HYDROCHLORIDE)
EQ 1MG BASE
Marketing Status: Discontinued

Active Ingredient: ANAGRELIDE HYDROCHLORIDE
Proprietary Name: ANAGRELIDE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 1MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A076530
Product Number: 002
Approval Date: Apr 18, 2005
Applicant Holder Full Name: BARR LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information