NDC codes

FDA NDC Directory
Product NDC (as listed)72162-1425Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-1425Add 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
72162-1425-272162142502721621425026 BOTTLE, SPRAY in 1 CARTON (72162-1425-2) / 1 SPRAY in 1 BOTTLE, SPRAY (72162-1425-4)Marketed from Apr 3, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
zolmitriptan
Generic name (nonproprietary)
zolmitriptan
Active ingredients
Zolmitriptan — 5 mg/1
Dosage form
Spray
Route
Nasal
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212469
Marketing start
Listing expires
Other FDA classes
Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
Identifiers
Product ID 72162-1425_0beab896-668c-44fe-bc69-3d0f7837cd1eSPL ID 0beab896-668c-44fe-bc69-3d0f7837cd1eSPL set ID e304c986-24fa-451e-a560-0af658ba387bRxCUI 402000UNII 2FS66TH3YW
Pharmacologic class
Serotonin-1b and Serotonin-1d Receptor Agonist

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

N472162142502 followed by a unit qualifier and the quantity

Package 72162-1425-02. 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)

Zolmitriptan Nasal Spray is indicated for the acute treatment of migraine with or without aura in adults and pediatric patients 12 years of age and older. Limitations of Use: • Only use zolmitriptan if a clear diagnosis of migraine has been established. If a patient has no response to zolmitriptan treatment for the first migraine attack, reconsider the diagnosis of migraine before zolmitriptan is administered to treat any subsequent attacks. • Zolmitriptan is not indicated for the prevention of migraine attacks. • Safety and effectiveness of zolmitriptan have not been established for cluster headache. • Not recommended in patients with moderate or severe hepatic impairment [ see Dosage and A…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-1425

What is NDC 72162-1425?
72162-1425 is the product NDC for zolmitriptan, Zolmitriptan 5 mg/1 spray, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
zolmitriptan.
What is the active ingredient?
Zolmitriptan.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for zolmitriptan?
37 other product NDCs are listed under this name. See all zolmitriptan NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other zolmitriptan NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ZolmitriptanZolmitriptan 2.5 mg/1Spray, MeteredNasalAmneal Pharmaceuticals NY LLC69238-235169238-2351-06
ZolmitriptanZolmitriptan 5 mg/1Spray, MeteredNasalAmneal Pharmaceuticals NY LLC69238-235269238-2352-06
ZolmitriptanZolmitriptan 2.5 mg/1Tablet, Orally disintegratingOralAlembic Pharmaceuticals Inc.62332-18162332-0181-06
ZolmitriptanZolmitriptan 5 mg/1Tablet, Orally disintegratingOralAlembic Pharmaceuticals Inc.62332-18262332-0182-03
ZolmitriptanZolmitriptan 2.5 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Inc.62332-46262332-0462-06
ZolmitriptanZolmitriptan 5 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Inc.62332-46362332-0463-03
ZolmitriptanZolmitriptan 2.5 mg/1TabletOralDirect_Rx72189-43472189-0434-06
ZolmitriptanZolmitriptan 5 mg/1TabletOralDirect_Rx72189-43572189-0435-03
zolmitriptanZolmitriptan 5 mg/1SprayNasalPadagis Israel Pharmaceuticals Ltd45802-71145802-0711-91
zolmitriptanZolmitriptan 5 mg/1SprayNasalBryant Ranch Prepack63629-957563629-9575-01

All 38 zolmitriptan NDCs

Other NDCs under ANDA 212469

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

FDA NDC Directory listings under ANDA 212469
ProductStrengthForm · routeLabelerProduct NDC
zolmitriptanZolmitriptan 5 mg/1SprayNasalPadagis Israel Pharmaceuticals Ltd45802-711
zolmitriptanZolmitriptan 5 mg/1SprayNasalBryant Ranch Prepack63629-9575
zolmitriptanZolmitriptan 5 mg/1SprayNasalBryant Ranch Prepack71335-2947

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