Active Ingredient: AMINOPHYLLINE
Proprietary Name: AMINOPHYLLINE
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A084575
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: IMPAX LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information