Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 072668

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TIMOLOL MALEATE (TIMOLOL MALEATE)
5MG
Marketing Status: Prescription

Active Ingredient: TIMOLOL MALEATE
Proprietary Name: TIMOLOL MALEATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A072668
Product Number: 002
Approval Date: Jun 8, 1990
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:  Prescription
Patent and Exclusivity Information

TIMOLOL MALEATE (TIMOLOL MALEATE)
10MG
Marketing Status: Prescription

Active Ingredient: TIMOLOL MALEATE
Proprietary Name: TIMOLOL MALEATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A072668
Product Number: 003
Approval Date: Jun 8, 1990
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:  Prescription
Patent and Exclusivity Information

TIMOLOL MALEATE (TIMOLOL MALEATE)
20MG
Marketing Status: Prescription

Active Ingredient: TIMOLOL MALEATE
Proprietary Name: TIMOLOL MALEATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A072668
Product Number: 001
Approval Date: Jun 8, 1990
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:  Prescription
Patent and Exclusivity Information