Suppliers / Bioindustria L.I.M

Bioindustria L.I.M

Italy Updated 9 July 2026

Bioindustria L.I.M is an API manufacturer based in Italy. It holds 6 valid CEPs across a filed portfolio of 6 molecules.

0
active US DMFs
6
valid CEPs
1
registered plants
24
filings across 1 regulators

Registered plants

Site FDA FEI
Novi Ligure, Italy Not on file

What they file, and where

Molecule Regulators Docs
Indapamide EDQM, SFDA (Saudi Arabia) 2
Amiloride EDQM 1
Baclofen EDQM 1
Dobutamine EDQM 1
Tamsulosin EDQM 1
Torasemide EDQM 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
AIFA (IT) 24 None

Questions about Bioindustria L.I.M

Does Bioindustria L.I.M hold a US DMF or a CEP?
Bioindustria L.I.M holds 6 valid CEPs. 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.
Where does Bioindustria L.I.M manufacture?
1 registered site is on record, in Italy (Novi Ligure). Every site is listed on this page with the register it came from.
What does Bioindustria L.I.M make?
6 molecules are on record against Bioindustria L.I.M, including Indapamide, Amiloride, Baclofen and Dobutamine. Each links through to that molecule's full manufacturer list.
Where does Bioindustria L.I.M file?
Filings are on record with AIFA (IT), 24 in total.

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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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability