E-Z-Paque (barium sulfate) NDC 32909-750

NDC codes

FDA NDC Directory

Product NDC (as listed)32909-750Labeler and product segments. Claims need a package NDC.

Product NDC at billing width32909-0750Add 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
32909-750-03	32909075003	24 BOTTLE, PLASTIC in 1 CARTON (32909-750-03) / 176 g in 1 BOTTLE, PLASTICMarketed from Jun 1, 2017

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): E-Z-Paque
Generic name (nonproprietary): barium sulfate
Active ingredients: Barium sulfate — 960 mg/g
Dosage form: Powder, For suspension
Route: Oral
Labeler: E-Z-EM Canada Inc
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 208036
Marketing start: Jun 1, 2017
Listing expires: Dec 31, 2027
Other FDA classes: X-Ray Contrast Activity (Mechanism)
Identifiers: Product ID 32909-750_03c905f1-817f-4562-b222-50859241cbdeSPL ID 03c905f1-817f-4562-b222-50859241cbdeSPL set ID 7225868a-4037-c96a-44e3-3326d36cbedcUNII 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

N432909075003 followed by a unit qualifier and the quantity

Package 32909-0750-03. 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)

E-Z-PAQUE is indicated for use in single contrast radiographic examinations of the esophagus, stomach, duodenum and small bowel to visualize the gastrointestinal tract (GI) in adult and pediatric patients. E-Z-PAQUE is a radiographic contrast agent indicated for use in single contrast radiographic examinations of the esophagus, stomach, duodenum and small bowel to visualize 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)

Other NDCs under NDA 208036

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

FDA NDC Directory listings under NDA 208036
Product	Strength	Form · route	Labeler	Product NDC
Varibar Thin Liquidbarium sulfate	Barium sulfate .81 g/g	Powder, For suspensionOral	E-Z-EM Canada Inc	32909-105
E-Z-HDbarium sulfate	Barium sulfate 980 mg/g	Powder, For suspensionOral	E-Z-EM Canada Inc	32909-764