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Approved Drug Products containing 17532 listed in the FDA Orange Book. Original Data : FDA Website

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01 3SANOFI AVENTIS US

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PharmaCompass

01

Brand Name : DIABETA

Sanofi

Dosage Form : TABLET; ORAL

Proprietary Name : DIABETA

Dosage Strength : 5MG

Approval Date : 1984-05-01

Application Number : 17532

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB2

Sanofi Company Banner

02

Brand Name : DIABETA

Sanofi

Dosage Form : TABLET; ORAL

Proprietary Name : DIABETA

Dosage Strength : 1.25MG

Approval Date : 1984-05-01

Application Number : 17532

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB2

Sanofi Company Banner

03

Brand Name : DIABETA

Sanofi

Dosage Form : TABLET; ORAL

Proprietary Name : DIABETA

Dosage Strength : 2.5MG

Approval Date : 1984-05-01

Application Number : 17532

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB2

Sanofi Company Banner