Suppliers / Aalidhra Pharmachem

Aalidhra Pharmachem

India 113 employees Updated 9 July 2026

Aalidhra Pharmachem is an API manufacturer based in India. It holds 3 valid CEPs across a filed portfolio of 3 molecules. Its GMP standing is certified by CDSCO (India). Customs aggregates show $210K of exports covering 20 molecules to 6 destinations in 2025.

0
active US DMFs
3
valid CEPs
2
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Nandesari, India Not on file
Vadodara, India Not on file

What they file, and where

Molecule Regulators Docs
Fenofibrate EDQM 1
Lacosamide EDQM 1
Pregabalin EDQM 1

Also appears on these molecule pages

Fenofibrate API Pregabalin API Lacosamide API

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $45K 3
2025 Not reported $210K 6
2024 Not reported $177K 3
2023 Not reported $50K 2

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 We do not publish the identity of any buyer.

Questions about Aalidhra Pharmachem

Does Aalidhra Pharmachem hold a US DMF or a CEP?
Aalidhra Pharmachem holds 3 valid CEPs. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Aalidhra Pharmachem manufacture?
2 registered sites are on record, in India (Nandesari and Vadodara). Every site is listed on this page with the register it came from.
What does Aalidhra Pharmachem make?
3 molecules are on record against Aalidhra Pharmachem, including Fenofibrate, Lacosamide and Pregabalin. Each links through to that molecule's full manufacturer list.
Which regulators recognise Aalidhra Pharmachem'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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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