Suppliers / Auro Laboratories

Auro Laboratories

India 55 employees Updated 9 July 2026

Auro Laboratories is an API manufacturer based in India. It holds 2 valid CEPs across a filed portfolio of 2 molecules. Its GMP standing is certified by EMA. Customs aggregates show $3.2M of exports covering 113 molecules to 19 destinations in 2025.

0
active US DMFs
2
valid CEPs
2
registered plants
4
filings across 1 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
Mumbai, India Not on file
Thane, India Not on file

What they file, and where

Molecule Regulators Docs
Metformin EDQM, SFDA (Saudi Arabia) 2
Chlorpheniramine EDQM 1

Also appears on these molecule pages

Chlorphenamine API Chlorpheniramine API Chlorzoxazone contract manufacturing Glimepiride contract manufacturing Glipizide contract manufacturing Metformin contract manufacturing

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 4 None
EMA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $393K 9
2025 Not reported $3.2M 19
2024 Not reported $1.6M 21
2023 Not reported $4.0M 19

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 We do not publish the identity of any buyer.

Questions about Auro Laboratories

Does Auro Laboratories hold a US DMF or a CEP?
Auro Laboratories holds 2 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 Auro Laboratories manufacture?
2 registered sites are on record, in India (Mumbai and Thane). Every site is listed on this page with the register it came from.
What does Auro Laboratories make?
2 molecules are on record against Auro Laboratories, including Metformin and Chlorpheniramine. Each links through to that molecule's full manufacturer list.
Which regulators recognise Auro Laboratories'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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Comparable suppliers

Specgx shares 2 molecules Supriya Lifescience shares 2 molecules Malladi Drugs & Pharmaceuticals shares 2 molecules Far Specialty Products Inc Dba Far Chemical shares 2 molecules Kongo Chemical shares 2 molecules

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