Active Ingredient: CHLORTHALIDONE
Proprietary Name: CHLORTHALIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A089286
Product Number: 002
Approval Date: Jul 21, 1986
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information
