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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 022198

SANCUSO (GRANISETRON)
3.1MG/24HR
Marketing Status: Prescription
Active Ingredient: GRANISETRON
Proprietary Name: SANCUSO
Dosage Form; Route of Administration: FILM, EXTENDED RELEASE; TRANSDERMAL
Strength: 3.1MG/24HR
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N022198
Product Number: 001
Approval Date: Sep 12, 2008
Applicant Holder Full Name: CUMBERLAND PHARMACEUTICALS INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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