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LITHIUM CARBONATE - 16590-781-90 - (LITHIUM CARBONATE)

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Drug Information of LITHIUM CARBONATE

Product NDC: 16590-781
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: 16590-781
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018558
Marketing Category: NDA
Start Marketing Date: 19820129

Package Information of LITHIUM CARBONATE

Package NDC: 16590-781-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (16590-781-90)

NDC Information of LITHIUM CARBONATE

NDC Code 16590-781-90
Proprietary Name LITHIUM CARBONATE
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (16590-781-90)
Product NDC 16590-781
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LITHIUM CARBONATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19820129
Marketing Category Name NDA
Labeler Name STAT RX USA LLC
Substance Name LITHIUM CARBONATE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Mood Stabilizer [EPC]

Complete Information of LITHIUM CARBONATE


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