NDC codes

FDA NDC Directory
Product NDC (as listed)71863-123Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71863-0123Add 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 NDC11-digit (billing)PackageCopy
71863-123-147186301231471863012314145 mL in 1 BOTTLE (71863-123-14)Marketed from Mar 2, 2026

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)
Desmoda
Generic name (nonproprietary)
desmopressin acetate oral solution
Active ingredients
Desmopressin acetate — .05 mg/mL
Dosage form
Solution
Route
Oral
Labeler
Eton Pharmaceuticals, Inc.NDC labeler code 71863
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 219873
Marketing start
Listing expires
Other FDA classes
Increased Coagulation Factor VIII Activity (Physiologic effect)Increased Coagulation Factor VIII Concentration (Physiologic effect)Vasopressins (Chemical structure)
Identifiers
Product ID 71863-123_4c0e1356-d150-cfb4-e063-6294a90acd27SPL ID 4c0e1356-d150-cfb4-e063-6294a90acd27SPL set ID 4c0e1356-d14f-cfb4-e063-6294a90acd27RxCUI 2738083, 2738090UNII XB13HYU18UUPC 0371863123145
Pharmacologic class
Factor VIII Activator; Vasopressin Analog

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

N471863012314 followed by a unit qualifier and the quantity

Package 71863-0123-14. 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 .

Indications (excerpt from the label)

DESMODA is indicated for the management of central diabetes insipidus as antidiuretic replacement therapy for adults and pediatric patients. Limitations of Use • DESMODA is not indicated for the treatment of nephrogenic diabetes insipidus. DESMODA is a vasopressin analog indicated for the management of central diabetes insipidus as antidiuretic replacement therapy for adults and pediatric patients. Limitations of Use • DESMODA is not indicated for the treatment of nephrogenic diabetes insipidus.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71863-123

What is NDC 71863-123?
71863-123 is the product NDC for Desmoda (desmopressin acetate oral solution), Desmopressin acetate .05 mg/mL solution, listed with the FDA by Eton Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Desmoda (Desmopressin Acetate Oral Solution).
What is the active ingredient?
Desmopressin acetate.
Who is the labeler?
Eton Pharmaceuticals, Inc., NDC labeler code 71863. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Desmoda?
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.

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