Suppliers / Par Laboratories 34

Par Laboratories 34

India Updated 9 July 2026

Par Laboratories 34 is a finished-dose manufacturer based in India. It appears in 4 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by CDSCO (India).

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

Registered plants

Site FDA FEI
gozaria 382 825 mehsana, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 4 None
CDSCO (India) None 2

Questions about Par Laboratories 34

Does Par Laboratories 34 hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Par Laboratories 34. It does have 4 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Par Laboratories 34 manufacture?
1 registered site is on record, in India (Gozaria 382 825 Mehsana). Every site is listed on this page with the register it came from.
Which regulators recognise Par Laboratories 34's GMP?
Current GMP certificates are on record from CDSCO (India). 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