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Lithium Carbonate - 65977-5046-0 - (Lithium Carbonate)

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Drug Information of Lithium Carbonate

Product NDC: 65977-5046
Proprietary Name: Lithium Carbonate
Non Proprietary Name: Lithium Carbonate
Active Ingredient(s): 600    mg/1 & nbsp;   Lithium Carbonate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Lithium Carbonate

Product NDC: 65977-5046
Labeler Name: Hetero Drugs Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090702
Marketing Category: ANDA
Start Marketing Date: 20090925

Package Information of Lithium Carbonate

Package NDC: 65977-5046-0
Package Description: 30 CAPSULE in 1 BOTTLE (65977-5046-0)

NDC Information of Lithium Carbonate

NDC Code 65977-5046-0
Proprietary Name Lithium Carbonate
Package Description 30 CAPSULE in 1 BOTTLE (65977-5046-0)
Product NDC 65977-5046
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lithium Carbonate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20090925
Marketing Category Name ANDA
Labeler Name Hetero Drugs Limited
Substance Name LITHIUM CARBONATE
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Mood Stabilizer [EPC]

Complete Information of Lithium Carbonate


General Information