Is E-Z-EM Canada Inc FDA approved?

E-Z-EM Canada Inc holds 1 FDA-registered establishment in Canada. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.

Where are E-Z-EM Canada Inc's drugs manufactured?

The FDA register lists Anjou. Registered operations: analytical testing, labelling, finished drug manufacture, packaging.

What drugs does E-Z-EM Canada Inc make?

18 products are listed under E-Z-EM Canada Inc in the openFDA NDC Directory, most often as suspension; powder, for suspension; cream. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

E-Z-EM Canada Inc

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 1
Active NDC listings: 18
Labeller names: 2
Live patents: 0
Countries: 1
Base: Canada

Authorisation

Registered operations

Analytical testing1Labelling1Finished drug manufacture1Packaging1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
E-Z-EM Canada Inc	11065 L.H. Lafontaine Blvd, Anjou, Quebec H1J2Z4, Canada (CAN)	Analytical testing, Labelling, Finished drug manufacture, Packaging	3002808342204211163

Catalogue

Drug listings by form and route

18 active NDC listings: 17 human prescription drug, 1 human otc drug. By marketing category: NDA 16, OTC MONOGRAPH DRUG 1, UNAPPROVED DRUG OTHER 1.

Dosage form	NDCs
suspension	11
powder, for suspension	3
cream	1
granule, effervescent	1
paste	1
tablet	1

Route	NDCs
oral	18

Labeller name on the listing	NDCs
e-z-em canada inc	16
e-z-em, inc.	2

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
E-Z-Disk	barium sulfate	tablet, oral	10361-778NDA
E-Z-GAS II	Antacid/AntiFlatulent	granule, effervescent, oral	10361-793OTC MONOGRAPH DRUG
E-Z-HD	barium sulfate	powder, for suspension, oral	32909-764NDA
E-Z-Paque	barium sulfate	suspension, oral	32909-187NDA
E-Z-Paque	barium sulfate	powder, for suspension, oral	32909-750NDA
E-Z-Paste	Barium Sulfate	cream, oral	32909-770UNAPPROVED DRUG OTHER
ENTERO Vu 24%	barium sulfate	suspension, oral	32909-146NDA
Readi-Cat 2	Barium Sulfate	suspension, oral	32909-744NDA
Readi-Cat 2 Banana Smoothie	Barium Sulfate	suspension, oral	32909-742NDA
Readi-Cat 2 Berry Smoothie	Barium Sulfate	suspension, oral	32909-741NDA
Readi-Cat 2 Creamy Vanilla Smoothie	Barium Sulfate	suspension, oral	32909-746NDA
Readi-Cat 2 Mochaccino Smoothie	Barium Sulfate	suspension, oral	32909-747NDA
Tagitol V	Barium Sulfate	suspension, oral	32909-814NDA
Varibar Honey	barium sulfate	suspension, oral	32909-122NDA
Varibar Nectar	barium sulfate	suspension, oral	32909-116NDA
Varibar Pudding	Barium Sulfate	paste, oral	32909-125NDA
Varibar Thin Honey	barium sulfate	suspension, oral	32909-121NDA
Varibar Thin Liquid	barium sulfate	powder, for suspension, oral	32909-105NDA

Neighbours

Registered in the same town

Laboratoire Atlas IncAnjou, CAN

Compare

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Novocol Pharmaceutical of Canada, Inc.1 site · 12 NDC
Diversey Canada, Inc1 site · 9 NDC
Natures Formulae Health Products Ltd.1 site · 9 NDC
Laboratoires Delon1 site · 6 NDC

Enquiry

Common questions

Is E-Z-EM Canada Inc FDA approved?: E-Z-EM Canada Inc holds 1 FDA-registered establishment in Canada. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are E-Z-EM Canada Inc's drugs manufactured?: The FDA register lists Anjou. Registered operations: analytical testing, labelling, finished drug manufacture, packaging.
What drugs does E-Z-EM Canada Inc make?: 18 products are listed under E-Z-EM Canada Inc in the openFDA NDC Directory, most often as suspension; powder, for suspension; cream. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.