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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 017697

KINEVAC (SINCALIDE)
0.005MG/VIAL
Marketing Status: Prescription
Active Ingredient: SINCALIDE
Proprietary Name: KINEVAC
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.005MG/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N017697
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: BRACCO DIAGNOSTICS INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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