Suppliers / Medley Pharmaceuticals

Medley Pharmaceuticals

India 3 duplicate records merged Updated 9 July 2026

Medley Pharmaceuticals is a finished-dose manufacturer based in India. It appears in 127 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with DAV (Vietnam), ZAMRA (ZM) and UZPHARM (UZ). Its GMP standing is certified by DRAP (PK), CDSCO (India) and NAFDAC (NG). Customs aggregates show $17.4M of exports covering 1,997 molecules to 21 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
127
filings across 6 regulators

Registered plants

Site FDA FEI
Kachigam, India Not on file
wah, Pakistan Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 58 None
ZAMRA (ZM) 31 None
UZPHARM (UZ) 18 None
TMDA (TZ) 12 None
NAFDAC (NG) 6 1
EFDA (ET) 2 None
DRAP (PK) None 1
CDSCO (India) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $3.0M 13
2025 Not reported $17.4M 21
2024 Not reported $22.0M 24
2023 Not reported $15.4M 22

Export figures are customs aggregates. We do not publish the identity of any buyer.

Questions about Medley Pharmaceuticals

Does Medley Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Medley Pharmaceuticals. It does have 127 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Medley Pharmaceuticals manufacture?
2 registered sites are on record, in India and Pakistan (Kachigam and Wah). Every site is listed on this page with the register it came from.
Which regulators recognise Medley Pharmaceuticals's GMP?
Current GMP certificates are on record from DRAP (PK), CDSCO (India) 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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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates
Customs aggregates
Export values, molecule and destination counts