Last Updated: September 24, 2026

Details for New Drug Application (NDA): 072542

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NDA 072542 describes LITHIUM CARBONATE, which is a drug marketed by Able, Alembic Ltd, Apotex Inc, Glenmark Pharms Ltd, Hetero Labs Ltd Iii, Hikma, Pharmobedient, Usl Pharma, Watson Labs, Alembic, Glenmark Pharms, Heritage Pharma, Hikma Intl Pharms, Unique, Pfizer, and Sun Pharm Inds Inc, and is included in twenty-nine NDAs. It is available from twenty suppliers. Additional details are available on the LITHIUM CARBONATE profile page.

The generic ingredient in LITHIUM CARBONATE is lithium carbonate. There is one drug master file entry for this compound. Twenty-one suppliers are listed for this compound. Additional details are available on the lithium carbonate profile page.

Summary for 072542

Tradename:	LITHIUM CARBONATE
Applicant:	Usl Pharma
Ingredient:	lithium carbonate
Patents:	0

Medical Subject Heading (MeSH) Categories for 072542

Antidepressive Agents
Antimanic Agents
Enzyme Inhibitors

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	CAPSULE;ORAL			Strength	300MG
Approval Date:	Feb 1, 1989	TE:		RLD:	No

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