Home > National Drug Code (NDC) > Lithium Carbonate

Lithium Carbonate - 49349-691-02 - (Lithium Carbonate)

Alphabetical Index


Drug Information of Lithium Carbonate

Product NDC: 49349-691
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: 49349-691
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076691
Marketing Category: ANDA
Start Marketing Date: 20110517

Package Information of Lithium Carbonate

Package NDC: 49349-691-02
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (49349-691-02)

NDC Information of Lithium Carbonate

NDC Code 49349-691-02
Proprietary Name Lithium Carbonate
Package Description 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (49349-691-02)
Product NDC 49349-691
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lithium Carbonate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110517
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name LITHIUM CARBONATE
Strength Number 450
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lithium Carbonate


General Information