What is NDC 71335-2983?

71335-2983 is the product NDC for Eletriptan hydrobromide, Eletriptan hydrobromide 40 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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 71335-2983

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2983Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2983Add 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
71335-2983-1	71335298301	30 TABLET, FILM COATED in 1 BOTTLE (71335-2983-1)Marketed from Feb 4, 2026

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): Eletriptan hydrobromide
Generic name (nonproprietary): eletriptan hydrobromide
Active ingredients: Eletriptan hydrobromide — 40 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 206409
Marketing start: Jul 12, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
Identifiers: Product ID 71335-2983_1d19d99c-189e-4065-97e8-78e357d62f60SPL ID 1d19d99c-189e-4065-97e8-78e357d62f60SPL set ID 7924b4fa-3e3d-4777-a59f-9320c6118196RxCUI 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

N471335298301 followed by a unit qualifier and the quantity

Package 71335-2983-01. 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 Feb 4, 2026.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2983

What is NDC 71335-2983?: 71335-2983 is the product NDC for Eletriptan hydrobromide, Eletriptan hydrobromide 40 mg/1 tablet, film coated, 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?: Eletriptan hydrobromide.
What is the active ingredient?: Eletriptan hydrobromide.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 71335. 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 20 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-104	59651-0104-69
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

All 17 Eletriptan hydrobromide NDCs

Other NDCs under ANDA 206409

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

FDA NDC Directory listings under ANDA 206409
Product	Strength	Form · route	Labeler	Product NDC
Eletriptan hydrobromide	Eletriptan hydrobromide 20 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	68382-922
Eletriptan hydrobromide	Eletriptan hydrobromide 40 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	68382-923
Eletriptan hydrobromide	Eletriptan hydrobromide 20 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1107
Eletriptan hydrobromide	Eletriptan hydrobromide 40 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1108