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Approved Drug Products containing 21392 listed in the FDA Orange Book. Original Data : FDA Website

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01 6BAUSCH

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PharmaCompass

01

Brand Name : CARDIZEM LA

Discovery on Target
Not Confirmed
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Brand Name : CARDIZEM LA

Discovery on Target
Not Confirmed
arrow

Bausch & Lomb Incorporated

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : CARDIZEM LA

Dosage Strength : 360MG

Approval Date : 2003-02-06

Application Number : 21392

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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02

Brand Name : CARDIZEM LA

Discovery on Target
Not Confirmed
arrow

Brand Name : CARDIZEM LA

Discovery on Target
Not Confirmed
arrow

Bausch & Lomb Incorporated

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : CARDIZEM LA

Dosage Strength : 240MG

Approval Date : 2003-02-06

Application Number : 21392

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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03

Brand Name : CARDIZEM LA

Discovery on Target
Not Confirmed
arrow

Brand Name : CARDIZEM LA

Discovery on Target
Not Confirmed
arrow

Bausch & Lomb Incorporated

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : CARDIZEM LA

Dosage Strength : 120MG

Approval Date : 2003-02-06

Application Number : 21392

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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04

Brand Name : CARDIZEM LA

Discovery on Target
Not Confirmed
arrow

Brand Name : CARDIZEM LA

Discovery on Target
Not Confirmed
arrow

Bausch & Lomb Incorporated

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : CARDIZEM LA

Dosage Strength : 420MG

Approval Date : 2003-02-06

Application Number : 21392

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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05

Brand Name : CARDIZEM LA

Discovery on Target
Not Confirmed
arrow

Brand Name : CARDIZEM LA

Discovery on Target
Not Confirmed
arrow

Bausch & Lomb Incorporated

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : CARDIZEM LA

Dosage Strength : 300MG

Approval Date : 2003-02-06

Application Number : 21392

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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06

Brand Name : CARDIZEM LA

Discovery on Target
Not Confirmed
arrow

Brand Name : CARDIZEM LA

Discovery on Target
Not Confirmed
arrow

Bausch & Lomb Incorporated

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : CARDIZEM LA

Dosage Strength : 180MG

Approval Date : 2003-02-06

Application Number : 21392

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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