What is NDC 10361-778?

10361-778 is the product NDC for E-Z-Disk (barium sulfate), Barium sulfate 700 mg/1 tablet, listed with the FDA by E-Z-EM, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

E-Z-EM, INC., NDC labeler code 10361. 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-Disk?

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-Disk NDC 10361-778 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)10361-778Labeler and product segments. Claims need a package NDC.

Product NDC at billing width10361-0778Add 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
10361-778-31	10361077831	100 TABLET in 1 BOTTLE, GLASS (10361-778-31)Marketed from Feb 1, 2009

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-Disk
Generic name (nonproprietary): barium sulfate
Active ingredients: Barium sulfate — 700 mg/1
Dosage form: Tablet
Route: Oral
Labeler: E-Z-EM, INC.NDC labeler code 10361
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 219840
Marketing start: Feb 1, 2009
Listing expires: Dec 31, 2026
Other FDA classes: X-Ray Contrast Activity (Mechanism)
Identifiers: Product ID 10361-778_29014e07-78d9-38c1-1945-8cb44ec6f69bSPL ID 29014e07-78d9-38c1-1945-8cb44ec6f69bSPL set ID c759668b-5cf1-b237-00c8-a5e4733b6f4cUNII 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

N410361077831 followed by a unit qualifier and the quantity

Package 10361-0778-31. 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 Sep 29, 2025.

Indications (excerpt from the label)

E-Z-DISK is indicated for the evaluation of esophageal patency in adults and pediatric patients aged 12 years and older. E-Z-DISK is a radiographic contrast agent indicated for the evaluation of esophageal patency in adults and pediatric patients aged 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 10361-778

What is NDC 10361-778?: 10361-778 is the product NDC for E-Z-Disk (barium sulfate), Barium sulfate 700 mg/1 tablet, listed with the FDA by E-Z-EM, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: E-Z-Disk (Barium sulfate).
What is the active ingredient?: Barium sulfate.
Who is the labeler?: E-Z-EM, INC., NDC labeler code 10361. 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-Disk?: 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.

E-Z-Disk (Barium sulfate) NDC 10361-778