Prescription drug · ANDA
Ethosuximide NDC 42806-711
Ethosuximide 250 mg/1 · Capsule · Oral · Epic Pharma, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 42806-711-01 | 4280607110142806071101 | 100 CAPSULE in 1 BOTTLE (42806-711-01)Marketed from Apr 15, 2020 |
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
- Listing expires
- Other FDA classes
- Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
- Identifiers
- Product ID 42806-711_2b366128-2db7-bb4e-e063-6294a90af2d7SPL ID 2b366128-2db7-bb4e-e063-6294a90af2d7SPL set ID a040dab2-0d70-4c02-a830-5ba1e3506a1bRxCUI 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
N442806071101followed by a unit qualifier and the quantityPackage 42806-0711-01. 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)
INDICATIONS AND USAGE Ethosuximide is indicated for the control of absence (petit mal) epilepsy.
Excerpt only. Read the full label for complete information.
About NDC 42806-711
- What is NDC 42806-711?
- 42806-711 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.
Related NDCs: other Ethosuximide products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Ethosuximide | Ethosuximide 250 mg/1 | CapsuleOral | Epic Pharma, LLC | 42806-708 | 42806-0708-01 |
| 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.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Ethosuximide | Ethosuximide 250 mg/1 | CapsuleOral | Epic Pharma, LLC | 42806-708 |