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Lithium Carbonate - 0143-3188-01 - (Lithium Carbonate)

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Drug Information of Lithium Carbonate

Product NDC: 0143-3188
Proprietary Name: Lithium Carbonate
Non Proprietary Name: Lithium Carbonate
Active Ingredient(s): 150    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: 0143-3188
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076243
Marketing Category: ANDA
Start Marketing Date: 20030301

Package Information of Lithium Carbonate

Package NDC: 0143-3188-01
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (0143-3188-01)

NDC Information of Lithium Carbonate

NDC Code 0143-3188-01
Proprietary Name Lithium Carbonate
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (0143-3188-01)
Product NDC 0143-3188
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lithium Carbonate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20030301
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
Substance Name LITHIUM CARBONATE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Mood Stabilizer [EPC]

Complete Information of Lithium Carbonate


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