LITHOBID (LITHIUM CARBONATE)
Summary
FDA approved LITHOBID (LITHIUM CARBONATE) by ANI PHARMS. NDA (New Drug) approval (Labeling) on 2022-10-13. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
NDA018027-69
Action Date
2022-10-13
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
LITHOBID (generic: LITHIUM CARBONATE), TABLET, EXTENDED RELEASE, ORAL. Application: NDA018027
Company
Context & Analysis
ANI PHARMS has 27 FDA actions in our database.
Frequently Asked Questions
How often does ANI PHARMS have FDA actions?
ANI PHARMS has 27 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA018027-69" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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