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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: A074501
Product Number: 001
Approval Date: Nov 9, 1995
Applicant Holder Full Name: SANDOZ INC
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: NADOLOL
Proprietary Name: NADOLOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 40MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A074501
Product Number: 002
Approval Date: Nov 9, 1995
Applicant Holder Full Name: SANDOZ INC
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: NADOLOL
Proprietary Name: NADOLOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 80MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A074501
Product Number: 003
Approval Date: Nov 9, 1995
Applicant Holder Full Name: SANDOZ INC
Marketing Status:
Prescription
Patent and Exclusivity Information