Active Ingredient: NALOXONE HYDROCHLORIDE
Proprietary Name: NALOXONE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.4MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A070649
Product Number: 001
Approval Date: Nov 17, 1986
Applicant Holder Full Name: ABRAXIS PHARMACEUTICAL PRODUCTS
Marketing Status:
Discontinued
Patent and Exclusivity Information