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Active Ingredient: NADOLOL
Proprietary Name: NADOLOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 80MG
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A074368
Product Number: 001
Approval Date: Aug 31, 1994
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: NADOLOL
Proprietary Name: NADOLOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 120MG
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A074368
Product Number: 002
Approval Date: Aug 31, 1994
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: NADOLOL
Proprietary Name: NADOLOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 160MG
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A074368
Product Number: 003
Approval Date: Aug 31, 1994
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status:
Discontinued
Patent and Exclusivity Information