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Lithium Carbonate - 51079-180-20 - (lithium carbonate)

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Drug Information of Lithium Carbonate

Product NDC: 51079-180
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, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Lithium Carbonate

Product NDC: 51079-180
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202288
Marketing Category: ANDA
Start Marketing Date: 20120810

Package Information of Lithium Carbonate

Package NDC: 51079-180-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-180-20) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-180-01)

NDC Information of Lithium Carbonate

NDC Code 51079-180-20
Proprietary Name Lithium Carbonate
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-180-20) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-180-01)
Product NDC 51079-180
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lithium carbonate
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120810
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
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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