Active Ingredient: NALOXONE HYDROCHLORIDE
Proprietary Name: NALOXONE HYDROCHLORIDE
Dosage Form; Route of Administration: SPRAY, METERED; NASAL
Strength: 4MG/SPRAY
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A209522
Product Number: 001
Approval Date: Apr 19, 2019
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status:
Over-the-counter
Patent and Exclusivity Information
