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Serving hundreds of leading biopharmaceutical companies globally:

Healthtrust
Queensland Health
Medtronic
Boehringer Ingelheim
Daiichi Sankyo
AstraZeneca
McKinsey
US Department of Justice
Cantor Fitzgerald

Generated: June 23, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 016834

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NDA 016834 describes LITHIUM CARBONATE, which is a drug marketed by Able, Alembic Ltd, Apotex Inc, Glenmark Generics, Hetero Labs Ltd Iii, Mylan Pharms Inc, Usl Pharma, Watson Labs, West-ward Pharms Int, Alembic Pharms Ltd, Barr, Glenmark Pharms Inc, Heritage Pharma, Hikma Intl Pharms, Unique Pharm Labs, Pfizer, and Sun Pharm Inds Inc, and is included in twenty-nine NDAs. It is available from thirty-two suppliers. Additional details are available on the LITHIUM CARBONATE profile page.

The generic ingredient in LITHIUM CARBONATE is lithium carbonate. There are fifteen drug master file entries for this compound. Thirty-three suppliers are listed for this compound. Additional details are available on the lithium carbonate profile page.
Summary for 016834
Tradename:LITHIUM CARBONATE
Applicant:Pfizer
Ingredient:lithium carbonate
Patents:0
Therapeutic Class:Bipolar Agents
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 016834

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength300MG
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

US Department of Justice
Moodys
Fuji
Baxter
Covington
Merck
Chubb
Fish and Richardson
Healthtrust

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