Suppliers / Livent Usa

Livent Usa

United States Updated 9 July 2026

Livent Usa is an API manufacturer based in United States. It holds one active US drug master file. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 11 September 2025 as NAI.

1
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
6 of 6 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 11 September 2025 NAI US FDA
  • 7 February 2020 VAI US FDA
  • 16 February 2018 VAI US FDA
  • 27 September 2016 NAI US FDA
  • 2 May 2013 NAI US FDA
  • 20 April 2010 NAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Bessemer City, United States 1015213

What they file, and where

Molecule Regulators Docs
Lithium Carbonate SFDA (Saudi Arabia), US FDA 2

Also appears on these molecule pages

Lithium Carbonate API

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1

Questions about Livent Usa

Does Livent Usa hold a US DMF or a CEP?
Livent Usa holds 1 active US drug master file. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Is Livent Usa FDA-registered?
One site operated by Livent Usa carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Livent Usa's last inspection go?
The most recent inspection on record closed on 11 September 2025 as NAI (No Action Indicated: nothing objectionable was found). 6 inspections are on file.
Where does Livent Usa manufacture?
1 registered site is on record, in United States (Bessemer City). Every site is listed on this page with the register it came from.
What does Livent Usa make?
1 molecule is on record against Livent Usa, including Lithium Carbonate. Each links through to that molecule's full manufacturer list.
Which regulators recognise Livent Usa's GMP?
Current GMP certificates are on record from US FDA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Open risk flags

  • The most recent inspection outcome was NAI, on 11 September 2025.

Comparable suppliers

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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates