Suppliers / Baader Schulz Laboratories

Baader Schulz Laboratories

India 38 employees Updated 9 July 2026

Baader Schulz Laboratories is a finished-dose manufacturer based in India. It appears in 13 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with NAFDAC (NG) and FDA (GH). Its GMP standing is certified by NAFDAC (NG), CDSCO (India) and FDA (GH). Customs aggregates show $329K of exports covering 26 molecules to 3 destinations in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants
13
filings across 2 regulators

Registered plants

Site FDA FEI
Dabhel, India Not on file
daman, India Not on file
OIDC Mahatma Gandhi Udyog Nagar-Daman, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 11 2
FDA (GH) 2 1
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2025 Not reported $329K 3
2024 Not reported $271K 3
2023 Not reported $190K 3
2022 Not reported $647K 3

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 We do not publish the identity of any buyer.

Questions about Baader Schulz Laboratories

Does Baader Schulz Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Baader Schulz Laboratories. It does have 13 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Baader Schulz Laboratories manufacture?
3 registered sites are on record, in India and Nigeria (Dabhel, Daman and Oidc Mahatma Gandhi Udyog Nagar-daman). Every site is listed on this page with the register it came from.
Which regulators recognise Baader Schulz Laboratories's GMP?
Current GMP certificates are on record from NAFDAC (NG), CDSCO (India) and FDA (GH). 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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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