Suppliers / Indus Pharma

Indus Pharma

Pakistan 997 employees Updated 9 July 2026

Indus Pharma is a finished-dose manufacturer based in Pakistan. It appears in 8 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with JFDA (JO), DAV (Vietnam) and TMDA (TZ). Its GMP standing is certified by DRAP (PK) and EAEU_EEC.

0
active US DMFs
0
valid CEPs
1
registered plants
8
filings across 3 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
karachi, Pakistan Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
JFDA (JO) 4 None
DAV (Vietnam) 2 None
TMDA (TZ) 2 None
DRAP (PK) None 1
EAEU_EEC None 1

Questions about Indus Pharma

Does Indus Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Indus Pharma. It does have 8 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Indus Pharma manufacture?
1 registered site is on record, in Pakistan (Karachi). Every site is listed on this page with the register it came from.
Which regulators recognise Indus Pharma's GMP?
Current GMP certificates are on record from DRAP (PK) and EEC (Eurasian Economic Union). 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