Suppliers / Gangwal Healthcare

Gangwal Healthcare

India 166 employees Updated 9 July 2026

Gangwal Healthcare is a contract manufacturer based in India. It holds 2 active US drug master files across a filed portfolio of 2 molecules. Customs aggregates show $2.0M of exports covering 199 molecules to 33 destinations in 2025.

2
active US DMFs
0
valid CEPs
0
registered plants
1
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Isoxsuprine US FDA 1
Salmeterol US FDA 1

Also appears on these molecule pages

Formoterol contract manufacturing Modafinil contract manufacturing Salmeterol contract manufacturing Timolol contract manufacturing

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 1 None

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $239K 10
2025 Not reported $2.0M 33
2024 Not reported $652K 26
2023 Not reported $562K 20

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 We do not publish the identity of any buyer.

Questions about Gangwal Healthcare

Does Gangwal Healthcare hold a US DMF or a CEP?
Gangwal Healthcare holds 2 active US drug master files. 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.
What does Gangwal Healthcare make?
2 molecules are on record against Gangwal Healthcare, including Isoxsuprine and Salmeterol. Each links through to that molecule's full manufacturer list.
Where does Gangwal Healthcare file?
Filings are on record with MINSA (CR), 1 in total.

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

MSN Laboratories shares 1 molecule Cipla shares 1 molecule Neuland Laboratories shares 1 molecule Natco Pharma shares 1 molecule Industriale Chimica shares 1 molecule

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
Customs aggregates
Export values, molecule and destination counts