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LITHIUM CARBONATE - 54868-3632-0 - (Lithium Carbonate)

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Drug Information of LITHIUM CARBONATE

Product NDC: 54868-3632
Proprietary Name: LITHIUM CARBONATE
Non Proprietary Name: Lithium Carbonate
Active Ingredient(s): 150    mg/1 & nbsp;   Lithium Carbonate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of LITHIUM CARBONATE

Product NDC: 54868-3632
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090702
Marketing Category: ANDA
Start Marketing Date: 20051205

Package Information of LITHIUM CARBONATE

Package NDC: 54868-3632-0
Package Description: 100 CAPSULE in 1 BOTTLE (54868-3632-0)

NDC Information of LITHIUM CARBONATE

NDC Code 54868-3632-0
Proprietary Name LITHIUM CARBONATE
Package Description 100 CAPSULE in 1 BOTTLE (54868-3632-0)
Product NDC 54868-3632
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lithium Carbonate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20051205
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name LITHIUM CARBONATE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Mood Stabilizer [EPC]

Complete Information of LITHIUM CARBONATE


General Information