Suppliers / Dr. Reddy's

Dr. Reddy's

India 88 employees Updated 9 July 2026

The public registers hold a second record for Dr. Reddy's. The fuller profile, with 279 active US DMFs and 90 valid CEPs, is at Dr Reddy's Laboratories. Figures on this page cover only this record.

Dr. Reddy's is an API and finished-dose manufacturer based in India. It appears in 714 regulatory filings across 13 regulators, without an active US DMF or CEP on file. Its filings concentrate with AIFA (IT), MEDSAFE (NZ) and INHRR (VE). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
2
registered plants
714
filings across 13 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
Noord-Holland, Netherlands Not on file
DK-2665 VALLENSBÆK STRAND, Norway Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
AIFA (IT) 330 None
MEDSAFE (NZ) 137 None
INHRR (VE) 106 None
EMA 36 1
DKMA (DK) 28 None
MPA (SE) 18 None

Questions about Dr. Reddy's

Does Dr. Reddy's hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Dr. Reddy's. It does have 714 filings with 13 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Dr. Reddy's manufacture?
2 registered sites are on record, in Netherlands and Norway (Noord-holland and Dk-2665 Vallensbæk Strand). Every site is listed on this page with the register it came from.
What does Dr. Reddy's make?
2 molecules are on record against Dr. Reddy's, including Esomeprazole and Metformin. Each links through to that molecule's full manufacturer list.
Which regulators recognise Dr. Reddy's's GMP?
Current GMP certificates are on record from EMA. 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