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Active Ingredient: TRICHLORMETHIAZIDE
Proprietary Name: METAHYDRIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: N012594
Product Number: 001
Approval Date: Jun 16, 1988
Applicant Holder Full Name: SANOFI AVENTIS US LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: TRICHLORMETHIAZIDE
Proprietary Name: METAHYDRIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 4MG
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: N012594
Product Number: 002
Approval Date: Jun 16, 1988
Applicant Holder Full Name: SANOFI AVENTIS US LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
