Active Ingredient: NADOLOL
Proprietary Name: NADOLOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A208832
Product Number: 001
Approval Date: Jun 2, 2017
Applicant Holder Full Name: AMNEAL PHARMACEUTICALS CO GMBH
Marketing Status:
Prescription
Patent and Exclusivity Information