Suppliers / Delhi Pharma, India

Delhi Pharma, India

India Updated 9 July 2026

Delhi Pharma, India is a finished-dose manufacturer based in India. It appears in 19 regulatory filings across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
0
registered plants
19
filings across 1 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 19 None

Limited public record

Beyond the filing counts above, the public registers hold no plant, inspection or portfolio detail for this company as at 9 July 2026. We report that as a gap rather than inferring an answer.

Questions about Delhi Pharma, India

Does Delhi Pharma, India hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Delhi Pharma, India. It does have 19 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Delhi Pharma, India file?
Filings are on record with DIGEMAPS (DO), 19 in total.

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