Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019574

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THALITONE (CHLORTHALIDONE)
15MG
Marketing Status: Prescription

Active Ingredient: CHLORTHALIDONE
Proprietary Name: THALITONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 15MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N019574
Product Number: 001
Approval Date: Dec 20, 1988
Applicant Holder Full Name: CASPER PHARMA LLC
Marketing Status:  Prescription
Patent and Exclusivity Information

THALITONE (CHLORTHALIDONE)
25MG
Marketing Status: Prescription

Active Ingredient: CHLORTHALIDONE
Proprietary Name: THALITONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: BX
Application Number: N019574
Product Number: 002
Approval Date: Feb 12, 1992
Applicant Holder Full Name: CASPER PHARMA LLC
Marketing Status:  Prescription
Patent and Exclusivity Information