Suppliers / Gobbi Novag

Gobbi Novag

Argentina Updated 9 July 2026

Gobbi Novag is a finished-dose manufacturer based in Argentina. It appears in 46 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANMAT (AR) and MINSA (CR). Customs aggregates show $1.6M of exports covering 54 molecules to 5 destinations in 2025.

0
active US DMFs
0
valid CEPs
1
registered plants
46
filings across 2 regulators

Registered plants

Site FDA FEI
BUENOS AIRES, Argentina Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANMAT (AR) 44 None
MINSA (CR) 2 None

Scale

Year Revenue Exports Destinations
2025 Not reported $1.6M 5
2024 Not reported $598K 5
2023 Not reported $466K 6
2022 Not reported $536K 3

Export figures are customs aggregates. We do not publish the identity of any buyer.

Questions about Gobbi Novag

Does Gobbi Novag hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Gobbi Novag. It does have 46 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Gobbi Novag manufacture?
1 registered site is on record, in Argentina (Buenos Aires). Every site is listed on this page with the register it came from.
Where does Gobbi Novag file?
Filings are on record with ANMAT (AR) and MINSA (CR), 46 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
Customs aggregates
Export values, molecule and destination counts