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Data / Drug companies / E-Z-Em Canada Inc

E-Z-Em Canada Inc: 16 products in the FDA NDC directory, labeler code 32909

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

E-Z-Em Canada Inc (labeler code 32909) lists 16 products in the FDA National Drug Code Directory, covering 1 finished drug by generic name. By type: 16 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on November 1, 2020.

The request: Watch E-Z-Em Canada Inc (FDA labeler code 32909): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
32909
Products in commercial distribution
16
Packages
19
Finished drugs by generic name
1
Prescription products
16
Over the counter products
0
Flagged as original packager
16 of 16 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
June 1, 1974
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
New drug applications (NDA)1593.8%
Other unapproved drugs16.2%

Products by type

TypeProductsShare
Prescription drugs16100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Barium sulfate162

Dosage forms

Dosage formProductsShare
Suspension1168.8%
Powder, for suspension318.8%
Cream16.2%
Paste16.2%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Readi-Cat 2 Mochaccino Smoothie32909-747SuspensionNew drug applications (NDA)November 1, 2020
Readi-Cat 2 Creamy Vanilla Smoothie32909-746SuspensionNew drug applications (NDA)November 1, 2020
Readi-Cat 232909-744SuspensionNew drug applications (NDA)November 1, 2020
Readi-Cat 2 Banana Smoothie32909-742SuspensionNew drug applications (NDA)November 1, 2020
Readi-Cat 2 Berry Smoothie32909-741SuspensionNew drug applications (NDA)November 1, 2020
E-Z-Paque32909-187SuspensionNew drug applications (NDA)November 1, 2020
Varibar Nectar32909-116SuspensionNew drug applications (NDA)November 1, 2020
ENTERO Vu 24%32909-146SuspensionNew drug applications (NDA)October 1, 2020
Varibar Thin Liquid32909-105Powder, for suspensionNew drug applications (NDA)April 30, 2019
Varibar Honey32909-122SuspensionNew drug applications (NDA)March 1, 2018
Varibar Thin Honey32909-121SuspensionNew drug applications (NDA)January 3, 2018
Tagitol V32909-814SuspensionNew drug applications (NDA)August 4, 2017
E-Z-Paque32909-750Powder, for suspensionNew drug applications (NDA)June 1, 2017
Varibar Pudding32909-125PasteNew drug applications (NDA)October 14, 2016
E-z-hd32909-764Powder, for suspensionNew drug applications (NDA)January 11, 2016
E-Z-Paste32909-770CreamOther unapproved drugsJune 1, 1974

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.