What is NDC 59651-104?

59651-104 is the product NDC for Eletriptan Hydrobromide, Eletriptan hydrobromide 20 mg/1 tablet, film coated, listed with the FDA by Aurobindo Pharma Limited. It has 1 package NDC, shown above in 10- and 11-digit form.

Aurobindo Pharma Limited, NDC labeler code 59651. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Eletriptan Hydrobromide NDC 59651-104 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59651-104Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59651-0104Add 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
59651-104-69	59651010469	1 BLISTER PACK in 1 CARTON (59651-104-69) / 6 TABLET, FILM COATED in 1 BLISTER PACK (59651-104-06)Marketed from Jan 15, 2019

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 — 20 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Aurobindo Pharma LimitedNDC labeler code 59651
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210708
Marketing start: Jan 15, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
Identifiers: Product ID 59651-104_f505017a-a5d7-4f9a-a62f-06a28b30f645SPL ID f505017a-a5d7-4f9a-a62f-06a28b30f645SPL set ID bb5ea5df-4add-420d-88cb-6dabe116ca65RxCUI 359493, 359494UNII M41W832TA3UPC 0359651105696
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

N459651010469 followed by a unit qualifier and the quantity

Package 59651-0104-69. 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 Jun 3, 2024.

Indications (excerpt from the label)

Eletriptan hydrobromide tablets are indicated for the acute treatment of migraine with or without aura in adults. 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 diagnosis of migraine before eletriptan hydrobromide tablets are administered to treat any subsequent attacks. Eletriptan hydrobromide tablets are not intended for the prevention of migraine attacks. Safety and effectiveness of eletriptan hydrobromide tablets have not been established for cluster headache. Eletriptan hydrobromide is a serotonin (5-HT 1B/1D ) receptor agonist (trip…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59651-104

What is NDC 59651-104?: 59651-104 is the product NDC for Eletriptan Hydrobromide, Eletriptan hydrobromide 20 mg/1 tablet, film coated, listed with the FDA by Aurobindo Pharma Limited. 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?: Aurobindo Pharma Limited, NDC labeler code 59651. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Eletriptan Hydrobromide	Eletriptan hydrobromide 20 mg/1	Tablet, Film coatedOral	Apnar Pharma LP	24689-167	24689-0167-01
Eletriptan Hydrobromide	Eletriptan hydrobromide 40 mg/1	Tablet, Film coatedOral	Apnar Pharma LP	24689-168	24689-0168-01
Eletriptan hydrobromide	Eletriptan hydrobromide 20 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-443	31722-0443-31
Eletriptan hydrobromide	Eletriptan hydrobromide 40 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-444	31722-0444-3131722-0444-33
Eletriptan Hydrobromide	Eletriptan hydrobromide 40 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0408	80425-0408-01
Eletriptan Hydrobromide	Eletriptan hydrobromide 40 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-105	59651-0105-6959651-0105-93
Eletriptan Hydrobromide	Eletriptan hydrobromide 40 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-8320	63629-8320-0163629-8320-02
Eletriptan Hydrobromide	Eletriptan hydrobromide 20 mg/1	Tablet, Film coatedOral	Mylan Pharmaceuticals Inc.	0378-4287	00378-4287-85
Eletriptan Hydrobromide	Eletriptan hydrobromide 40 mg/1	Tablet, Film coatedOral	Mylan Pharmaceuticals Inc.	0378-4288	00378-4288-0800378-4288-85
Eletriptan Hydrobromide	Eletriptan hydrobromide 20 mg/1	Tablet, Film coatedOral	Teva Pharmaceuticals USA, Inc.	0093-8310	00093-8310-18

All 17 Eletriptan Hydrobromide NDCs

Other NDCs under ANDA 210708

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

FDA NDC Directory listings under ANDA 210708
Product	Strength	Form · route	Labeler	Product NDC
Eletriptan HBR	Eletriptan hydrobromide 40 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-517
Eletriptan Hydrobromide	Eletriptan hydrobromide 40 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-105
Eletriptan Hydrobromide	Eletriptan hydrobromide 40 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-8320
Eletriptan Hydrobromide	Eletriptan hydrobromide 40 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0408