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Lithium Carbonate - 0904-6136-60 - (Lithium Carbonate)

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Drug Information of Lithium Carbonate

Product NDC: 0904-6136
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): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Lithium Carbonate

Product NDC: 0904-6136
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076243
Marketing Category: ANDA
Start Marketing Date: 20030224

Package Information of Lithium Carbonate

Package NDC: 0904-6136-60
Package Description: 100 CAPSULE in 1 BOTTLE (0904-6136-60)

NDC Information of Lithium Carbonate

NDC Code 0904-6136-60
Proprietary Name Lithium Carbonate
Package Description 100 CAPSULE in 1 BOTTLE (0904-6136-60)
Product NDC 0904-6136
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lithium Carbonate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20030224
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name LITHIUM CARBONATE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Mood Stabilizer [EPC]

Complete Information of Lithium Carbonate


General Information