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Lithium Carbonate - 67544-534-70 - (Lithium Carbonate)

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Drug Information of Lithium Carbonate

Product NDC: 67544-534
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: 67544-534
Labeler Name: Aphena Pharma Solutions - Tennessee, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017812
Marketing Category: NDA
Start Marketing Date: 19801126

Package Information of Lithium Carbonate

Package NDC: 67544-534-70
Package Description: 120 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (67544-534-70)

NDC Information of Lithium Carbonate

NDC Code 67544-534-70
Proprietary Name Lithium Carbonate
Package Description 120 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (67544-534-70)
Product NDC 67544-534
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lithium Carbonate
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 19801126
Marketing Category Name NDA
Labeler Name Aphena Pharma Solutions - Tennessee, Inc.
Substance Name LITHIUM CARBONATE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Mood Stabilizer [EPC]

Complete Information of Lithium Carbonate


General Information