Suppliers / Allergan

Allergan

United States 5 duplicate records merged Updated 9 July 2026

Allergan is a finished-dose manufacturer based in United States. It appears in 122 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with Health Canada, INHRR (VE) and DMP (NO). Its GMP standing is certified by NAFDAC (NG).

0
active US DMFs
0
valid CEPs
1
registered plants
122
filings across 7 regulators

Registered plants

Site FDA FEI
Pringy, United Arab Emirates Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
Health Canada 84 None
INHRR (VE) 15 None
DMP (NO) 10 None
EDA (EG) 9 None
SFDA (Saudi Arabia) 2 None
NAFDAC (NG) 1 2

Questions about Allergan

Does Allergan hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Allergan. It does have 122 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Allergan manufacture?
1 registered site is on record, in United Arab Emirates (Pringy). Every site is listed on this page with the register it came from.
Which regulators recognise Allergan'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. Allergan comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

Aaa Pharmaceuticals also in United States Aarkish Pharmaceuticals NJ also in United States Abbott Laboratories also in United States Abon Pharmaceuticals also in United States Access Business Group also in United States

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