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Lithium Carbonate - 67046-430-30 - (Lithium Carbonate)

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Drug Information of Lithium Carbonate

Product NDC: 67046-430
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, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Lithium Carbonate

Product NDC: 67046-430
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017812
Marketing Category: NDA
Start Marketing Date: 20100406

Package Information of Lithium Carbonate

Package NDC: 67046-430-30
Package Description: 30 CAPSULE, GELATIN COATED in 1 BLISTER PACK (67046-430-30)

NDC Information of Lithium Carbonate

NDC Code 67046-430-30
Proprietary Name Lithium Carbonate
Package Description 30 CAPSULE, GELATIN COATED in 1 BLISTER PACK (67046-430-30)
Product NDC 67046-430
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lithium Carbonate
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20100406
Marketing Category Name NDA
Labeler Name Contract Pharmacy Services-PA
Substance Name LITHIUM CARBONATE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Mood Stabilizer [EPC]

Complete Information of Lithium Carbonate


General Information