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Active Ingredient: THIOTEPA
Proprietary Name: THIOTEPA
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 15MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A075698
Product Number: 001
Approval Date: Sep 20, 2001
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information