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LITHIUM CARBONATE - 54868-5239-0 - (Lithium Carbonate)

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Drug Information of LITHIUM CARBONATE

Product NDC: 54868-5239
Proprietary Name: LITHIUM CARBONATE
Non Proprietary Name: Lithium Carbonate
Active Ingredient(s): 300    mg/1 & nbsp;   Lithium Carbonate
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of LITHIUM CARBONATE

Product NDC: 54868-5239
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076832
Marketing Category: ANDA
Start Marketing Date: 20050301

Package Information of LITHIUM CARBONATE

Package NDC: 54868-5239-0
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5239-0)

NDC Information of LITHIUM CARBONATE

NDC Code 54868-5239-0
Proprietary Name LITHIUM CARBONATE
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5239-0)
Product NDC 54868-5239
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lithium Carbonate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20050301
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name LITHIUM CARBONATE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Mood Stabilizer [EPC]

Complete Information of LITHIUM CARBONATE


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