Suppliers / Mcneil and Argus Pharmaceuticals

Mcneil and Argus Pharmaceuticals

India Updated 9 July 2026

Mcneil and Argus Pharmaceuticals is a finished-dose manufacturer based in India. It appears in 6 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with NAFDAC (NG), FDA (GH) and ARCSA (EC). Its GMP standing is certified by SAHPRA (ZA), CDSCO (India) and NAFDAC (NG). Customs aggregates show $265 of exports covering 1 molecule to 1 destination in 2026 so far.

0
active US DMFs
0
valid CEPs
3
registered plants
6
filings across 5 regulators

Registered plants

Site FDA FEI
ambala cantt, India Not on file
Rampur, India Not on file
Sundumbili, South Africa Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 2 1
FDA (GH) 1 None
ARCSA (EC) 1 None
CDSCO (India) 1 2
ANPP (DZ) 1 None
SAHPRA (ZA) None 3

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $265 1

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 We do not publish the identity of any buyer.

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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