NDC codes

FDA NDC Directory
Product NDC (as listed)73352-096Labeler and product segments. Claims need a package NDC.
Product NDC at billing width73352-0096Add 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
73352-096-19733520096198 KIT in 1 KIT (73352-096-19) / 1 VIAL, GLASS in 1 KIT (73352-096-18) / 1 mL in 1 VIAL, GLASSMarketed from Jul 8, 2025

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)
Dihydroergotamine mesylate
Generic name (nonproprietary)
dihydroergotamine mesylate
Active ingredients
Dihydroergotamine mesylate — 4 mg/mL
Dosage form
Spray
Route
Nasal
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216881
Marketing start
Listing expires
Other FDA classes
Ergotamines (Chemical structure)
Identifiers
Product ID 73352-096_400914da-88c2-d003-e063-6394a90ad430SPL ID 400914da-88c2-d003-e063-6394a90ad430SPL set ID 4cb78f66-6ccf-4ac7-8599-e199f6995f05RxCUI 861668UNII 81AXN7R2QT
Pharmacologic class
Ergotamine Derivative

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. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N473352009619 followed by a unit qualifier and the quantity

Package 73352-0096-19. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Dihydroergotamine mesylate nasal spray is indicated for the acute treatment of migraine headaches with or without aura. Dihydroergotamine mesylate nasal spray is not intended for the prophylactic therapy of migraine or for the management of hemiplegic or basilar migraine.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 216881

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

FDA NDC Directory listings under ANDA 216881
ProductStrengthForm · routeLabelerProduct NDC
Dihydroergotamine mesylateDihydroergotamine mesylate 4 mg/mLSprayNasalAdvagen Pharma Ltd72888-096

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in