Active Ingredient: AMINOPHYLLINE
Proprietary Name: AMINOPHYLLINE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 25MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088407
Product Number: 001
Approval Date: Jan 25, 1984
Applicant Holder Full Name: ABRAXIS PHARMACEUTICAL PRODUCTS
Marketing Status:
Discontinued
Patent and Exclusivity Information