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Lithium Carbonate - 55154-4960-0 - (Lithium Carbonate)

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Drug Information of Lithium Carbonate

Product NDC: 55154-4960
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: 55154-4960
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076832
Marketing Category: ANDA
Start Marketing Date: 20041028

Package Information of Lithium Carbonate

Package NDC: 55154-4960-0
Package Description: 10 POUCH in 1 BAG (55154-4960-0) > 1 TABLET, EXTENDED RELEASE in 1 POUCH

NDC Information of Lithium Carbonate

NDC Code 55154-4960-0
Proprietary Name Lithium Carbonate
Package Description 10 POUCH in 1 BAG (55154-4960-0) > 1 TABLET, EXTENDED RELEASE in 1 POUCH
Product NDC 55154-4960
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lithium Carbonate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20041028
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name LITHIUM CARBONATE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Mood Stabilizer [EPC]

Complete Information of Lithium Carbonate


General Information