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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019129

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MAXZIDE (HYDROCHLOROTHIAZIDE; TRIAMTERENE)
50MG;75MG
Marketing Status: Prescription
Active Ingredient: HYDROCHLOROTHIAZIDE; TRIAMTERENE
Proprietary Name: MAXZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG;75MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N019129
Product Number: 001
Approval Date: Oct 22, 1984
Applicant Holder Full Name: AUROBINDO PHARMA USA INC
Marketing Status:  Prescription
Patent and Exclusivity Information
MAXZIDE-25 (HYDROCHLOROTHIAZIDE; TRIAMTERENE)
25MG;37.5MG
Marketing Status: Prescription
Active Ingredient: HYDROCHLOROTHIAZIDE; TRIAMTERENE
Proprietary Name: MAXZIDE-25
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG;37.5MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N019129
Product Number: 003
Approval Date: May 13, 1988
Applicant Holder Full Name: AUROBINDO PHARMA USA INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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