Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 072304

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ATENOLOL (ATENOLOL)
25MG
Marketing Status: Prescription

Active Ingredient: ATENOLOL
Proprietary Name: ATENOLOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A072304
Product Number: 002
Approval Date: Jul 31, 1992
Applicant Holder Full Name: TWI PHARMACEUTICALS INC
Marketing Status:  Prescription
Patent and Exclusivity Information

ATENOLOL (ATENOLOL)
50MG
Marketing Status: Prescription

Active Ingredient: ATENOLOL
Proprietary Name: ATENOLOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A072304
Product Number: 003
Approval Date: Jul 18, 1988
Applicant Holder Full Name: TWI PHARMACEUTICALS INC
Marketing Status:  Prescription
Patent and Exclusivity Information

ATENOLOL (ATENOLOL)
100MG
Marketing Status: Prescription

Active Ingredient: ATENOLOL
Proprietary Name: ATENOLOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A072304
Product Number: 001
Approval Date: Jul 15, 1988
Applicant Holder Full Name: TWI PHARMACEUTICALS INC
Marketing Status:  Prescription
Patent and Exclusivity Information