Active Ingredient: SAXAGLIPTIN HYDROCHLORIDE
Proprietary Name: SAXAGLIPTIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 2.5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A205941
Product Number: 001
Approval Date: Jul 31, 2023
Applicant Holder Full Name: AMNEAL PHARMACEUTICALS LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information