Active Ingredient: NALOXONE HYDROCHLORIDE
Proprietary Name: NALOXONE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.02MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A071672
Product Number: 001
Approval Date: Nov 17, 1987
Applicant Holder Full Name: SOLOPAK MEDICAL PRODUCTS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information