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Approved Drug Products containing 91544 listed in the FDA Orange Book. Original Data : FDA Website

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01 1GLENMARK PHARMS INC

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01

Brand Name : LITHIUM CARBONATE

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Brand Name : LITHIUM CARBONATE

Luxepack
Not Confirmed
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Glenmark Pharmaceuticals

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : LITHIUM CARBONATE

Dosage Strength : 300MG

Approval Date : 2010-12-27

Application Number : 91544

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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