Suppliers / Adcock Ingram

Adcock Ingram

South Africa Updated 9 July 2026

Adcock Ingram is a finished-dose manufacturer based in South Africa. It appears in 1,688 regulatory filings across 9 regulators, without an active US DMF or CEP on file. Its filings concentrate with SAHPRA (ZA), NMRC (NA) and MCAZ (ZW). Its GMP standing is certified by CDSCO (India), FDA (GH) and MCAZ (ZW), among 4 authorities. Customs aggregates show $45.8M of exports covering 1,889 molecules to 14 destinations in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants
1,688
filings across 9 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Bommasandra, India Not on file
Bengaluru, India Not on file
bengaluru 562 106, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
SAHPRA (ZA) 1,317 None
NMRC (NA) 302 None
MCAZ (ZW) 46 1
ZAMRA (ZM) 10 None
PPB (KE) 7 None
INVIMA (CO) 3 None
CDSCO (India) None 2
FDA (GH) None 2
EMA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $8.5M 9
2025 Not reported $45.8M 14
2024 $499.6M $58.4M 7
2023 $466.8M $50.2M 6
2022 $494.8M Not reported Not reported

Export figures are customs aggregates. We do not publish the identity of any buyer. Revenue shown in US dollars, converted from the reported currency.

Questions about Adcock Ingram

Does Adcock Ingram hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Adcock Ingram. It does have 1,688 filings with 9 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Adcock Ingram manufacture?
3 registered sites are on record, in India (Bommasandra, Bengaluru and Bengaluru 562 106). Every site is listed on this page with the register it came from.
Which regulators recognise Adcock Ingram's GMP?
Current GMP certificates are on record from CDSCO (India), FDA (GH), MCAZ (ZW) and EMA. 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
Company filings
Revenue as reported