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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019115

FENTANYL CITRATE (FENTANYL CITRATE)
EQ 0.05MG BASE/ML
Marketing Status: Prescription
Active Ingredient: FENTANYL CITRATE
Proprietary Name: FENTANYL CITRATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.05MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: N019115
Product Number: 001
Approval Date: Jan 12, 1985
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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