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 We do not publish the identity of any buyer.

Questions about Mcneil and Argus Pharmaceuticals

Does Mcneil and Argus Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Mcneil and Argus Pharmaceuticals. It does have 6 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Mcneil and Argus Pharmaceuticals manufacture?
3 registered sites are on record, in India and South Africa (Ambala Cantt, Rampur and Sundumbili). Every site is listed on this page with the register it came from.
Which regulators recognise Mcneil and Argus Pharmaceuticals's GMP?
Current GMP certificates are on record from SAHPRA (ZA), CDSCO (India) and NAFDAC (NG). 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