Suppliers / Delta Pharma

Delta Pharma

Pakistan 32 employees 4 duplicate records merged Updated 9 July 2026

Delta Pharma is a finished-dose manufacturer based in Pakistan. It appears in 371 regulatory filings across 11 regulators, without an active US DMF or CEP on file. Its filings concentrate with EDA (EG), INFARMED (PT) and NMRC (NA). Its GMP standing is certified by NAFDAC (NG), EDA (EG) and US FDA, among 4 authorities. Its most recent recorded inspection, by US FDA, closed on 15 August 2024 as VAI.

0
active US DMFs
0
valid CEPs
3
registered plants 1 with an FDA FEI number
371
filings across 11 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
4 of 4 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 15 August 2024 VAI US FDA
  • 16 November 2018 VAI US FDA
  • 30 October 2015 NAI US FDA
  • 9 February 2012 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Quebec, United Arab Emirates Not on file
Canada, Canada 3003264747
nowshera, Pakistan Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EDA (EG) 245 1
INFARMED (PT) 101 None
NMRC (NA) 5 None
EEC_EAEU 4 None
DIGEMAPS (DO) 4 None
NAFDAC (NG) 4 1
US FDA None 1
DRAP (PK) None 1

Scale

Year Revenue Exports Destinations
2025 $514K Not reported Not reported

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 We do not publish the identity of any buyer.

Questions about Delta Pharma

Does Delta Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Delta Pharma. It does have 371 filings with 11 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Delta Pharma FDA-registered?
One site operated by Delta Pharma carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Delta Pharma's last inspection go?
The most recent inspection on record closed on 15 August 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 4 inspections are on file.
Where does Delta Pharma manufacture?
3 registered sites are on record, in United Arab Emirates, Canada and Pakistan (Quebec, Canada and Nowshera). Every site is listed on this page with the register it came from.
Which regulators recognise Delta Pharma's GMP?
Current GMP certificates are on record from NAFDAC (NG), EDA (EG), US FDA and DRAP (PK). 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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Open risk flags

  • The most recent inspection outcome was VAI, on 15 August 2024.

Comparable suppliers

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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
Company filings
Revenue as reported