What is NDC 32909-744?

32909-744 is the product NDC for Readi-Cat 2 (barium sulfate), Barium sulfate 20 mg/mL suspension, listed with the FDA by E-Z-EM Canada Inc. It has 1 package NDC, shown above in 10- and 11-digit form.

E-Z-EM Canada Inc, NDC labeler code 32909. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Readi-Cat 2?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Readi-Cat 2 NDC 32909-744 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)32909-744Labeler and product segments. Claims need a package NDC.

Product NDC at billing width32909-0744Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
32909-744-03	32909074403	12 BOTTLE, PLASTIC in 1 CARTON (32909-744-03) / 450 mL in 1 BOTTLE, PLASTICMarketed from Nov 1, 2020

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Readi-Cat 2
Generic name (nonproprietary): barium sulfate
Active ingredients: Barium sulfate — 20 mg/mL
Dosage form: Suspension
Route: Oral
Labeler: E-Z-EM Canada IncNDC labeler code 32909
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 208143
Marketing start: Nov 1, 2020
Listing expires: Dec 31, 2027
Other FDA classes: X-Ray Contrast Activity (Mechanism)
Identifiers: Product ID 32909-744_57b0ef0b-4974-4d98-8fdf-22cef6245dd7SPL ID 57b0ef0b-4974-4d98-8fdf-22cef6245dd7SPL set ID d2d293d5-dcc9-0d3f-58ed-686ef0132d7cUNII 25BB7EKE2E
Pharmacologic class: Radiographic Contrast Agent

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N432909074403 followed by a unit qualifier and the quantity

Package 32909-0744-03. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Apr 15, 2026.

Indications (excerpt from the label)

READI-CAT 2 and READI-CAT 2 SMOOTHIES are indicated for use in computed tomography (CT) of the abdomen to delineate the gastrointestinal (GI) tract in adult and pediatric patients. READI-CAT 2 and READI-CAT 2 SMOOTHIE are radiographic contrast agents, indicated for use in computed tomography (CT) of the abdomen to delineate the gastrointestinal (GI) tract in adult and pediatric patients ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 32909-744

What is NDC 32909-744?: 32909-744 is the product NDC for Readi-Cat 2 (barium sulfate), Barium sulfate 20 mg/mL suspension, listed with the FDA by E-Z-EM Canada Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Readi-Cat 2 (Barium Sulfate).
What is the active ingredient?: Barium sulfate.
Who is the labeler?: E-Z-EM Canada Inc, NDC labeler code 32909. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Readi-Cat 2?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under NDA 208143

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under NDA 208143
Product	Strength	Form · route	Labeler	Product NDC
E-Z-Paquebarium sulfate	Barium sulfate .6 g/mL	SuspensionOral	E-Z-EM Canada Inc	32909-187
ENTERO Vu 24%barium sulfate	Barium sulfate 240 mg/mL	SuspensionOral	E-Z-EM Canada Inc	32909-146
Readi-Cat 2 Banana Smoothiebarium sulfate	Barium sulfate 20 mg/mL	SuspensionOral	E-Z-EM Canada Inc	32909-742
Readi-Cat 2 Berry Smoothiebarium sulfate	Barium sulfate 20 mg/mL	SuspensionOral	E-Z-EM Canada Inc	32909-741
Readi-Cat 2 Creamy Vanilla Smoothiebarium sulfate	Barium sulfate 20 mg/mL	SuspensionOral	E-Z-EM Canada Inc	32909-746
Readi-Cat 2 Mochaccino Smoothiebarium sulfate	Barium sulfate 20 mg/mL	SuspensionOral	E-Z-EM Canada Inc	32909-747
Tagitol Vbarium sulfate	Barium sulfate 400 mg/mL	SuspensionOral	E-Z-EM Canada Inc	32909-814
Varibar Honeybarium sulfate	Barium sulfate 400 mg/mL	SuspensionOral	E-Z-EM Canada Inc	32909-122
Varibar Nectarbarium sulfate	Barium sulfate 400 mg/mL	SuspensionOral	E-Z-EM Canada Inc	32909-116
Varibar Thin Honeybarium sulfate	Barium sulfate 400 mg/mL	SuspensionOral	E-Z-EM Canada Inc	32909-121

Readi-Cat 2 (Barium sulfate) NDC 32909-744