Suppliers / Saffron Pharmaceuticals - India

Saffron Pharmaceuticals - India

Pakistan 635 employees Updated 9 July 2026

Saffron Pharmaceuticals - India is a finished-dose manufacturer based in Pakistan. It appears in 18 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with NAFDAC (NG) and UZPHARM (UZ). Its GMP standing is certified by NAFDAC (NG).

0
active US DMFs
0
valid CEPs
1
registered plants
18
filings across 2 regulators

Registered plants

Site FDA FEI
Faisalabad-Pakistan, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 9 1
UZPHARM (UZ) 9 None

Questions about Saffron Pharmaceuticals - India

Does Saffron Pharmaceuticals - India hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Saffron Pharmaceuticals - India. It does have 18 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Saffron Pharmaceuticals - India manufacture?
1 registered site is on record, in Nigeria (Faisalabad-pakistan). Every site is listed on this page with the register it came from.
Which regulators recognise Saffron Pharmaceuticals - India's GMP?
Current GMP certificates are on record from 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.

Comparing suppliers?

Choose your molecules and target markets. Saffron Pharmaceuticals - India comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

Alliance Pharmaceuticals also in Pakistan Atco Laboratories also in Pakistan Brookes Pharma also in Pakistan Delta Pharma also in Pakistan Efroze Chemical Industries also in Pakistan

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