Suppliers / unique pharmaceutical laboratories

unique pharmaceutical laboratories

India 2 duplicate records merged Updated 9 July 2026

unique pharmaceutical laboratories is a finished-dose manufacturer based in India. It appears in 619 regulatory filings across 14 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), TMDA (TZ) and UZPHARM (UZ). Its GMP standing is certified by CDSCO (India), EMA and UZPHARM (UZ), among 6 authorities.

0
active US DMFs
0
valid CEPs
12
registered plants
619
filings across 14 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Daman, United Arab Emirates Not on file
Panoli / Gujarat, United Arab Emirates Not on file
Daman, United Arab Emirates Not on file
Daman, United Arab Emirates Not on file
Daman, United Arab Emirates Not on file
Panoli - 394 116, United Arab Emirates Not on file

6 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 410 None
TMDA (TZ) 51 None
UZPHARM (UZ) 39 2
EFDA (ET) 36 None
JFDA (JO) 17 None
DAV (Vietnam) 15 None
CDSCO (India) None 31
EMA None 3
ANVISA (Brazil) None 2
MHRA (UK) None 1
NAFDAC (NG) None 1

Questions about unique pharmaceutical laboratories

Does unique pharmaceutical laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for unique pharmaceutical laboratories. It does have 619 filings with 14 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does unique pharmaceutical laboratories manufacture?
12 registered sites are on record, in United Arab Emirates and India (Daman, Panoli / Gujarat and Panoli - 394 116 among others). Every site is listed on this page with the register it came from.
Which regulators recognise unique pharmaceutical laboratories's GMP?
Current GMP certificates are on record from CDSCO (India), EMA, UZPHARM (UZ), ANVISA (Brazil), MHRA (UK) and 1 more. 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