What is NDC 32909-764?

32909-764 is the product NDC for E-Z-HD (barium sulfate), Barium sulfate 980 mg/g powder, for 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 E-Z-HD?

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.

E-Z-HD NDC 32909-764 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)32909-764Labeler and product segments. Claims need a package NDC.

Product NDC at billing width32909-0764Add 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
32909-764-01	3290907640132909076401	24 BOTTLE in 1 CARTON (32909-764-01) / 340 g in 1 BOTTLEMarketed from Apr 18, 2016

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-HD
Generic name (nonproprietary): barium sulfate
Active ingredients: Barium sulfate — 980 mg/g
Dosage form: Powder, For suspension
Route: Oral
Labeler: E-Z-EM Canada IncNDC labeler code 32909
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 208036
Marketing start: Jan 11, 2016
Listing expires: Dec 31, 2027
Other FDA classes: X-Ray Contrast Activity (Mechanism)
Identifiers: Product ID 32909-764_c0b3cf2c-8b69-4c19-b436-41410d638424SPL ID c0b3cf2c-8b69-4c19-b436-41410d638424SPL set ID a4330804-7179-472a-91cb-84bbd5079bb8UNII 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

N432909076401 followed by a unit qualifier and the quantity

Package 32909-0764-01. 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-HD is indicated for use in double-contrast radiographic examinations of the esophagus, stomach and duodenum to help visualize the gastrointestinal (GI) tract in patients 12 years and older. E-Z-HD, a radiographic contrast agent, is indicated for use in double-contrast radiographic examinations of the esophagus, stomach and duodenum to visualize the gastrointestinal (GI) tract in patients 12 years and older ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 32909-764

What is NDC 32909-764?: 32909-764 is the product NDC for E-Z-HD (barium sulfate), Barium sulfate 980 mg/g powder, for 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?: E-Z-HD (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 E-Z-HD?: 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 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
E-Z-Paquebarium sulfate	Barium sulfate 960 mg/g	Powder, For suspensionOral	E-Z-EM Canada Inc	32909-750
Varibar Thin Liquidbarium sulfate	Barium sulfate .81 g/g	Powder, For suspensionOral	E-Z-EM Canada Inc	32909-105

E-Z-HD (Barium sulfate) NDC 32909-764