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Lithium Carbonate - 68462-220-11 - (Lithium Carbonate)

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Drug Information of Lithium Carbonate

Product NDC: 68462-220
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: 68462-220
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079139
Marketing Category: ANDA
Start Marketing Date: 20090203

Package Information of Lithium Carbonate

Package NDC: 68462-220-11
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (68462-220-11) > 10 CAPSULE in 1 BLISTER PACK

NDC Information of Lithium Carbonate

NDC Code 68462-220-11
Proprietary Name Lithium Carbonate
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (68462-220-11) > 10 CAPSULE in 1 BLISTER PACK
Product NDC 68462-220
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lithium Carbonate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20090203
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
Substance Name LITHIUM CARBONATE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Mood Stabilizer [EPC]

Complete Information of Lithium Carbonate


General Information