Suppliers / PHARMACIA & UPJOHN

PHARMACIA & UPJOHN

United States 2 duplicate records merged Updated 9 July 2026

PHARMACIA & UPJOHN is an API manufacturer based in United States. It holds 11 valid CEPs across a filed portfolio of 7 molecules. Its GMP standing is certified by MFDS (Korea).

0
active US DMFs
11
valid CEPs
2
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Kalamazoo, United States Not on file
Kalamazoo, United States Not on file

What they file, and where

Filings and GMP by regulator

Regulator Filings GMP certificates
MFDS (Korea) None 2

Questions about PHARMACIA & UPJOHN

Does PHARMACIA & UPJOHN hold a US DMF or a CEP?
PHARMACIA & UPJOHN holds 11 valid CEPs. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does PHARMACIA & UPJOHN manufacture?
2 registered sites are on record, in United States (Kalamazoo among others). Every site is listed on this page with the register it came from.
What does PHARMACIA & UPJOHN make?
7 molecules are on record against PHARMACIA & UPJOHN, including Dexamethasone, Hydrocortisone, Megestrol Acetate and Progesterone. Each links through to that molecule's full manufacturer list.
Which regulators recognise PHARMACIA & UPJOHN's GMP?
Current GMP certificates are on record from MFDS (Korea). 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