Suppliers / VPL Chemicals

VPL Chemicals

India Updated 9 July 2026

VPL Chemicals is an API manufacturer based in India. It holds 2 valid CEPs. Its GMP standing is certified by CDSCO (India). Customs aggregates show $2.4M of exports covering 261 molecules to 25 destinations in 2025.

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

Registered plants

Site FDA FEI
Bengaluru rural, India Not on file
bengaluru rural 562 111, India Not on file
Bengaluru Rural, India Not on file

What they file, and where

Molecule Regulators Docs
Minoxidil EDQM 2

Also appears on these molecule pages

Minoxidil API

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $631K 11
2025 Not reported $2.4M 25
2024 Not reported $2.1M 22
2023 Not reported $1.7M 21

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 We do not publish the identity of any buyer.

Questions about VPL Chemicals

Does VPL Chemicals hold a US DMF or a CEP?
VPL Chemicals 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 VPL Chemicals manufacture?
3 registered sites are on record, in India (Bengaluru Rural, Bengaluru Rural 562 111 and Bengaluru Rural). Every site is listed on this page with the register it came from.
What does VPL Chemicals make?
1 molecule is on record against VPL Chemicals, including Minoxidil. Each links through to that molecule's full manufacturer list.
Which regulators recognise VPL Chemicals'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