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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019353

ALFENTA (ALFENTANIL HYDROCHLORIDE)
EQ 0.5MG BASE/ML
Marketing Status: Prescription
Active Ingredient: ALFENTANIL HYDROCHLORIDE
Proprietary Name: ALFENTA
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.5MG BASE/ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N019353
Product Number: 001
Approval Date: Dec 29, 1986
Applicant Holder Full Name: RISING PHARMA HOLDINGS INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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