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Lithium Carbonate - 68462-224-10 - (Lithium Carbonate)

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Drug Information of Lithium Carbonate

Product NDC: 68462-224
Proprietary Name: Lithium Carbonate
Non Proprietary Name: Lithium Carbonate
Active Ingredient(s): 450    mg/1 & nbsp;   Lithium Carbonate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lithium Carbonate

Product NDC: 68462-224
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091616
Marketing Category: ANDA
Start Marketing Date: 20110214

Package Information of Lithium Carbonate

Package NDC: 68462-224-10
Package Description: 1000 TABLET in 1 BOTTLE (68462-224-10)

NDC Information of Lithium Carbonate

NDC Code 68462-224-10
Proprietary Name Lithium Carbonate
Package Description 1000 TABLET in 1 BOTTLE (68462-224-10)
Product NDC 68462-224
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lithium Carbonate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110214
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
Substance Name LITHIUM CARBONATE
Strength Number 450
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lithium Carbonate


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