Active Ingredient: DEXRAZOXANE HYDROCHLORIDE
Proprietary Name: DEXRAZOXANE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 250MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A076068
Product Number: 001
Approval Date: Sep 28, 2004
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: DEXRAZOXANE HYDROCHLORIDE
Proprietary Name: DEXRAZOXANE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A076068
Product Number: 002
Approval Date: Sep 28, 2004
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information