Suppliers / Laboratorios Biogalenic S A De C V

Laboratorios Biogalenic S A De C V

El Salvador Updated 9 July 2026

Laboratorios Biogalenic S A De C V is a finished-dose manufacturer based in El Salvador. It appears in 304 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with INHRR (VE), MINSA (CR) and ARCSA (EC).

0
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
304
filings across 3 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
El Salvador, El Salvador 3006785496

Filings and GMP by regulator

Regulator Filings GMP certificates
INHRR (VE) 294 None
MINSA (CR) 6 None
ARCSA (EC) 4 None

Questions about Laboratorios Biogalenic S A De C V

Does Laboratorios Biogalenic S A De C V hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorios Biogalenic S A De C V. It does have 304 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Laboratorios Biogalenic S A De C V FDA-registered?
One site operated by Laboratorios Biogalenic S A De C V 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.
Where does Laboratorios Biogalenic S A De C V manufacture?
1 registered site is on record, in El Salvador (El Salvador). Every site is listed on this page with the register it came from.
Where does Laboratorios Biogalenic S A De C V file?
Filings are on record with INHRR (VE), MINSA (CR) and ARCSA (EC), 304 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.

Comparing suppliers?

Choose your molecules and target markets. Laboratorios Biogalenic S A De C V comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Sources on this page

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