NDC codes

FDA NDC Directory
Product NDC (as listed)62135-790Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62135-0790Add 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
62135-790-126213507901262135079012120 CAPSULE in 1 BOTTLE (62135-790-12)Marketed from Oct 23, 2023

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
Chartwell RX, LLCNDC labeler code 62135
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 200892
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 62135-790_24119078-bcee-0aa9-e063-6394a90af9c8SPL ID 24119078-bcee-0aa9-e063-6394a90af9c8SPL set ID 43fdfd16-c723-452a-9c1d-accf6f7c622eRxCUI 197682UNII 5SEH9X1D1DUPC 0362135790127
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

N462135079012 followed by a unit qualifier and the quantity

Package 62135-0790-12. 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 capsule 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 62135-790

What is NDC 62135-790?
62135-790 is the product NDC for Ethosuximide, Ethosuximide 250 mg/1 capsule, listed with the FDA by Chartwell RX, 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?
Chartwell RX, LLC, NDC labeler code 62135. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
EthosuximideEthosuximide 250 mg/1CapsuleOralEpic Pharma, LLC42806-70842806-0708-01
EthosuximideEthosuximide 250 mg/1CapsuleOralEpic Pharma, LLC42806-71142806-0711-01
EthosuximideEthosuximide 250 mg/5mLSolutionOralMylan Pharmaceuticals Inc.59762-235059762-2350-0659762-2350-07
EthosuximideEthosuximide 250 mg/1CapsuleOralStrides Pharma Science Limited64380-87864380-0878-06
EthosuximideEthosuximide 250 mg/1Capsule, Liquid filledOralBryant Ranch Prepack63629-800563629-8005-01
EthosuximideEthosuximide 250 mg/1Capsule, Liquid filledOralBionpharma Inc.69452-15269452-0152-20
EthosuximideEthosuximide 250 mg/5mLSolutionOralChartwell RX, LLC62135-06462135-0064-47
EthosuximideEthosuximide 250 mg/5mLSolutionOralChartwell Governmental & Specialty RX, LLC.68999-06468999-0064-24
EthosuximideEthosuximide 250 mg/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-067000121-0670-16

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