Suppliers / Maps Laboratories

Maps Laboratories

India 24 employees Updated 9 July 2026

Maps Laboratories is an API manufacturer based in India. It holds 2 valid CEPs across a filed portfolio of 3 molecules. Its GMP standing is certified by CDSCO (India). Customs aggregates show $1.5M of exports covering 72 molecules to 14 destinations in 2025.

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

Registered plants

Site FDA FEI
Rafaleshwar, India Not on file
tal morbi jambudia 363 642 rajkot, India Not on file
rajkot, India Not on file

What they file, and where

Molecule Regulators Docs
Levocetirizine Dihydrochloride SFDA (Saudi Arabia) 1
Pregabalin EDQM 1
Trimetazidine Dihydrochloride EDQM 1

Also appears on these molecule pages

Levocetirizine API Trimetazidine API Pregabalin API

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) None 3

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $136K 8
2025 Not reported $1.5M 14
2024 Not reported $876K 12
2023 Not reported $1.9M 17

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 We do not publish the identity of any buyer.

Questions about Maps Laboratories

Does Maps Laboratories hold a US DMF or a CEP?
Maps 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 Maps Laboratories manufacture?
3 registered sites are on record, in India (Rafaleshwar, Tal Morbi Jambudia 363 642 Rajkot and Rajkot). Every site is listed on this page with the register it came from.
What does Maps Laboratories make?
3 molecules are on record against Maps Laboratories, including Levocetirizine Dihydrochloride, Pregabalin and Trimetazidine Dihydrochloride. Each links through to that molecule's full manufacturer list.
Which regulators recognise Maps Laboratories'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