Suppliers / Laboratorios Farma

Laboratorios Farma

Venezuela Updated 9 July 2026

Laboratorios Farma is a finished-dose manufacturer based in Venezuela. It appears in 317 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with INHRR (VE), ARCSA (EC) and EMA. Its GMP standing is certified by NAFDAC (NG).

0
active US DMFs
0
valid CEPs
1
registered plants
317
filings across 4 regulators

Registered plants

Site FDA FEI
Mortagua, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
INHRR (VE) 280 None
ARCSA (EC) 22 None
EMA 8 None
DIGEMAPS (DO) 7 None
NAFDAC (NG) None 1

Questions about Laboratorios Farma

Does Laboratorios Farma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorios Farma. It does have 317 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorios Farma manufacture?
1 registered site is on record, in Nigeria (Mortagua). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorios Farma's GMP?
Current GMP certificates are on record from NAFDAC (NG). 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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Sources on this page

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