What is NDC 42806-708?

42806-708 is the product NDC for Ethosuximide, Ethosuximide 250 mg/1 capsule, listed with the FDA by Epic Pharma, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Epic Pharma, LLC, NDC labeler code 42806. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Ethosuximide?

9 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ethosuximide NDC 42806-708 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)42806-708Labeler and product segments. Claims need a package NDC.

Product NDC at billing width42806-0708Add 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
42806-708-01	4280607080142806070801	100 CAPSULE in 1 BOTTLE (42806-708-01)Marketed from Nov 12, 2021

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): Ethosuximide
Generic name (nonproprietary): ethosuximide
Active ingredients: Ethosuximide — 250 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Epic Pharma, LLCNDC labeler code 42806
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210654
Marketing start: Nov 12, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers: Product ID 42806-708_2b206d5a-4881-923b-e063-6294a90a13b5SPL ID 2b206d5a-4881-923b-e063-6294a90a13b5SPL set ID 85c50760-98cc-4888-b27f-146937acc893RxCUI 197682UNII 5SEH9X1D1D
Pharmacologic class: Anti-epileptic Agent

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

N442806070801 followed by a unit qualifier and the quantity

Package 42806-0708-01. 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 Jan 7, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Ethosuximide is indicated for the control of absence (petit mal) epilepsy.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 42806-708

What is NDC 42806-708?: 42806-708 is the product NDC for Ethosuximide, Ethosuximide 250 mg/1 capsule, listed with the FDA by Epic Pharma, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Ethosuximide.
What is the active ingredient?: Ethosuximide.
Who is the labeler?: Epic Pharma, LLC, NDC labeler code 42806. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ethosuximide?: 9 other product NDCs are listed under this name. See all Ethosuximide 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 Ethosuximide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ethosuximide	Ethosuximide 250 mg/1	CapsuleOral	Epic Pharma, LLC	42806-711	42806-0711-01
Ethosuximide	Ethosuximide 250 mg/5mL	SolutionOral	Mylan Pharmaceuticals Inc.	59762-2350	59762-2350-0659762-2350-07
Ethosuximide	Ethosuximide 250 mg/1	CapsuleOral	Strides Pharma Science Limited	64380-878	64380-0878-06
Ethosuximide	Ethosuximide 250 mg/1	Capsule, Liquid filledOral	Bryant Ranch Prepack	63629-8005	63629-8005-01
Ethosuximide	Ethosuximide 250 mg/1	Capsule, Liquid filledOral	Bionpharma Inc.	69452-152	69452-0152-20
Ethosuximide	Ethosuximide 250 mg/1	CapsuleOral	Chartwell RX, LLC	62135-790	62135-0790-12
Ethosuximide	Ethosuximide 250 mg/5mL	SolutionOral	Chartwell RX, LLC	62135-064	62135-0064-47
Ethosuximide	Ethosuximide 250 mg/5mL	SolutionOral	Chartwell Governmental & Specialty RX, LLC.	68999-064	68999-0064-24
Ethosuximide	Ethosuximide 250 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-0670	00121-0670-16

Other NDCs under ANDA 210654

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

FDA NDC Directory listings under ANDA 210654
Product	Strength	Form · route	Labeler	Product NDC
Ethosuximide	Ethosuximide 250 mg/1	CapsuleOral	Epic Pharma, LLC	42806-711