NDC codes

FDA NDC Directory
Product NDC (as listed)24689-168Labeler and product segments. Claims need a package NDC.
Product NDC at billing width24689-0168Add 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
24689-168-012468901680124689016801100 TABLET, FILM COATED in 1 BOTTLE (24689-168-01)Marketed from May 13, 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)
Eletriptan Hydrobromide
Generic name (nonproprietary)
eletriptan hydrobromide
Active ingredients
Eletriptan hydrobromide — 40 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Apnar Pharma LPNDC labeler code 24689
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215467
Marketing start
Listing expires
Other FDA classes
Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
Identifiers
Product ID 24689-168_bf7e1524-0147-40cf-bd40-5ae994d551a6SPL ID bf7e1524-0147-40cf-bd40-5ae994d551a6SPL set ID 49686c51-bbd9-45f0-92b1-8ffa81612e35RxCUI 359493, 359494UNII M41W832TA3
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N424689016801 followed by a unit qualifier and the quantity

Package 24689-0168-01. 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 .

Indications (excerpt from the label)

Eletriptan Hydrobromide Tablets is indicated for the acute treatment of migraine with or without aura in adults. Eletriptan Hydrobromide Tablets is a serotonin (5-HT 1B/1D ) receptor agonist (triptan) indicated for the acute treatment of migraine with or without aura in adults ( 1 ) Limitations of Use: Use only after a clear diagnosis of migraine has been established ( 1 ) Not indicated for the prophylactic therapy of migraine ( 1 ) Not indicated for the treatment of cluster headache ( 1 ) Limitations of Use: Use only if a clear diagnosis of migraine has been established. If a patient has no response to the first migraine attack treated with Eletriptan Hydrobromide Tablets, reconsider the di…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 24689-168

What is NDC 24689-168?
24689-168 is the product NDC for Eletriptan Hydrobromide, Eletriptan hydrobromide 40 mg/1 tablet, film coated, listed with the FDA by Apnar Pharma LP. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Eletriptan Hydrobromide.
What is the active ingredient?
Eletriptan hydrobromide.
Who is the labeler?
Apnar Pharma LP, NDC labeler code 24689. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Eletriptan Hydrobromide?
16 other product NDCs are listed under this name. See all Eletriptan Hydrobromide 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 Eletriptan Hydrobromide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Eletriptan HydrobromideEletriptan hydrobromide 20 mg/1Tablet, Film coatedOralApnar Pharma LP24689-16724689-0167-01
Eletriptan hydrobromideEletriptan hydrobromide 20 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-44331722-0443-31
Eletriptan hydrobromideEletriptan hydrobromide 40 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-44431722-0444-3131722-0444-33
Eletriptan HydrobromideEletriptan hydrobromide 40 mg/1Tablet, Film coatedOralAdvanced Rx of Tennessee, LLC80425-040880425-0408-01
Eletriptan HydrobromideEletriptan hydrobromide 20 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-10459651-0104-69
Eletriptan HydrobromideEletriptan hydrobromide 40 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-10559651-0105-6959651-0105-93
Eletriptan HydrobromideEletriptan hydrobromide 40 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-832063629-8320-0163629-8320-02
Eletriptan HydrobromideEletriptan hydrobromide 20 mg/1Tablet, Film coatedOralMylan Pharmaceuticals Inc.0378-428700378-4287-85
Eletriptan HydrobromideEletriptan hydrobromide 40 mg/1Tablet, Film coatedOralMylan Pharmaceuticals Inc.0378-428800378-4288-0800378-4288-85
Eletriptan HydrobromideEletriptan hydrobromide 20 mg/1Tablet, Film coatedOralTeva Pharmaceuticals USA, Inc.0093-831000093-8310-18

All 17 Eletriptan Hydrobromide NDCs

Other NDCs under ANDA 215467

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

FDA NDC Directory listings under ANDA 215467
ProductStrengthForm · routeLabelerProduct NDC
Eletriptan HydrobromideEletriptan hydrobromide 20 mg/1Tablet, Film coatedOralApnar Pharma LP24689-167

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