Active Ingredient: HYDROCHLOROTHIAZIDE
Proprietary Name: HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: A083177
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: IVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA
Marketing Status:
Prescription
Patent and Exclusivity Information