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Lithium Carbonate - 0054-8528-25 - (Lithium Carbonate)

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Drug Information of Lithium Carbonate

Product NDC: 0054-8528
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): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lithium Carbonate

Product NDC: 0054-8528
Labeler Name: Roxane Laboratories, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA018558
Marketing Category: ANDA
Start Marketing Date: 19820614

Package Information of Lithium Carbonate

Package NDC: 0054-8528-25
Package Description: 10 TABLET in 1 BLISTER PACK (0054-8528-25)

NDC Information of Lithium Carbonate

NDC Code 0054-8528-25
Proprietary Name Lithium Carbonate
Package Description 10 TABLET in 1 BLISTER PACK (0054-8528-25)
Product NDC 0054-8528
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lithium Carbonate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19820614
Marketing Category Name ANDA
Labeler Name Roxane Laboratories, Inc
Substance Name LITHIUM CARBONATE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Mood Stabilizer [EPC]

Complete Information of Lithium Carbonate


General Information