Suppliers / Ranbaxy Pharmaceuticals {Pty)

Ranbaxy Pharmaceuticals {Pty)

South Africa 2 duplicate records merged Updated 9 July 2026

Ranbaxy Pharmaceuticals {Pty) is a finished-dose manufacturer based in South Africa. It appears in 194 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by SAHPRA (ZA).

0
active US DMFs
0
valid CEPs
1
registered plants
194
filings across 1 regulators

Registered plants

Site FDA FEI
Roodepoort, South Africa Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
SAHPRA (ZA) 194 3

Questions about Ranbaxy Pharmaceuticals {Pty)

Does Ranbaxy Pharmaceuticals {Pty) hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Ranbaxy Pharmaceuticals {Pty). It does have 194 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Ranbaxy Pharmaceuticals {Pty) manufacture?
1 registered site is on record, in South Africa (Roodepoort). Every site is listed on this page with the register it came from.
Which regulators recognise Ranbaxy Pharmaceuticals {Pty)'s GMP?
Current GMP certificates are on record from SAHPRA (ZA). 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