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Lithium Carbonate - 0904-6204-60 - (Lithium Carbonate)

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Drug Information of Lithium Carbonate

Product NDC: 0904-6204
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Lithium Carbonate

Product NDC: 0904-6204
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076490
Marketing Category: ANDA
Start Marketing Date: 20030617

Package Information of Lithium Carbonate

Package NDC: 0904-6204-60
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0904-6204-60)

NDC Information of Lithium Carbonate

NDC Code 0904-6204-60
Proprietary Name Lithium Carbonate
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0904-6204-60)
Product NDC 0904-6204
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lithium Carbonate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20030617
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name LITHIUM CARBONATE
Strength Number 450
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lithium Carbonate


General Information