Suppliers / Pliva Hrvatska d.o.o

Pliva Hrvatska d.o.o

Croatia Updated 9 July 2026

Pliva Hrvatska d.o.o is a finished-dose manufacturer based in Croatia. It appears in 101 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with US FDA, NCELS (KZ) and MPA (SE). Its GMP standing is certified by EAEU_EEC and NAFDAC (NG).

0
active US DMFs
0
valid CEPs
3
registered plants
101
filings across 6 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
0 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Загреб, Belarus Not on file
Загреб, Belarus Not on file
HR, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 72 None
NCELS (KZ) 13 None
MPA (SE) 7 None
RCETH (BY) 4 None
NAFDAC (NG) 3 2
UZPHARM (UZ) 2 None
EAEU_EEC None 2

Questions about Pliva Hrvatska d.o.o

Does Pliva Hrvatska d.o.o hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Pliva Hrvatska d.o.o. It does have 101 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Pliva Hrvatska d.o.o manufacture?
3 registered sites are on record, in Belarus and Nigeria (Загреб and HR among others). Every site is listed on this page with the register it came from.
Which regulators recognise Pliva Hrvatska d.o.o's GMP?
Current GMP certificates are on record from EEC (Eurasian Economic Union) and 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