Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 020439

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BETIMOL (TIMOLOL)
EQ 0.25% BASE
Marketing Status: Prescription

Active Ingredient: TIMOLOL
Proprietary Name: BETIMOL
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: EQ 0.25% BASE
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N020439
Product Number: 001
Approval Date: Mar 31, 1995
Applicant Holder Full Name: THEA PHARMA INC
Marketing Status:  Prescription
Patent and Exclusivity Information

BETIMOL (TIMOLOL)
EQ 0.5% BASE
Marketing Status: Prescription

Active Ingredient: TIMOLOL
Proprietary Name: BETIMOL
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: EQ 0.5% BASE
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N020439
Product Number: 002
Approval Date: Mar 31, 1995
Applicant Holder Full Name: THEA PHARMA INC
Marketing Status:  Prescription
Patent and Exclusivity Information