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Serving leading biopharmaceutical companies globally:

Covington
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Queensland Health
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Cerilliant
Daiichi Sankyo

Generated: December 11, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 076832

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NDA 076832 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-three 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-four suppliers are listed for this compound. Additional details are available on the lithium carbonate profile page.

Summary for 076832

Tradename:1
Applicant:1
Ingredient:1
Patents:0
Therapeutic Class:Bipolar Agents
Formulation / Manufacturing:see details

Pharmacology for NDA: 076832

Medical Subject Heading (MeSH) Categories for 076832

Suppliers and Packaging for NDA: 076832

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
LITHIUM CARBONATE lithium carbonate TABLET, EXTENDED RELEASE;ORAL 076832 ANDA West-Ward Pharmaceuticals Corp. 0054-0021 0054-0021-25 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0054-0021-25)
LITHIUM CARBONATE lithium carbonate TABLET, EXTENDED RELEASE;ORAL 076832 ANDA West-Ward Pharmaceuticals Corp. 0054-0021 0054-0021-29 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0054-0021-29)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrength300MG
Approval Date:Oct 28, 2004TE:ABRLD:No


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Serving leading biopharmaceutical companies globally:

Johnson and Johnson
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UBS
Citi
Argus Health
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US Army
AstraZeneca
Cerilliant
Fish and Richardson

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