Active Ingredient: PENTOXIFYLLINE
Proprietary Name: PENTOXIFYLLINE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 400MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A075199
Product Number: 001
Approval Date: Sep 3, 1999
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information