NDC codes

FDA NDC Directory
Product NDC (as listed)62135-660Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62135-0660Add 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
62135-660-606213506606060 TABLET in 1 BOTTLE, GLASS (62135-660-60)Marketed from Jun 21, 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)
Flecainide Acetate
Generic name (nonproprietary)
flecainide acetate
Active ingredients
Flecainide acetate — 50 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Chartwell RX, LLCNDC labeler code 62135
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 079164
Marketing start
Listing expires
Identifiers
Product ID 62135-660_25893d71-9846-59aa-e063-6294a90a3f48SPL ID 25893d71-9846-59aa-e063-6294a90a3f48SPL set ID a604aee4-30d5-4007-9882-98137d0d867fRxCUI 886662, 886666, 886671UNII M8U465Q1WQUPC 0362135661601, 0362135662608, 0362135660604
Pharmacologic class
Antiarrhythmic

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

N462135066060 followed by a unit qualifier and the quantity

Package 62135-0660-60. 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 In patients without structural heart disease, flecainide acetate is indicated for the prevention of — paroxysmal supraventricular tachycardias (PSVT), including atrioventricular nodal reentrant tachycardia, atrioventricular reentrant tachycardia and other supraventricular tachycardias of unspecified mechanism associated with disabling symptoms — paroxysmal atrial fibrillation/flutter (PAF) associated with disabling symptoms Flecainide acetate is also indicated for the prevention of — documented ventricular arrhythmias, such as sustained ventricular tachycardia ( sustained VT), that in the judgment of the physician are life-threatening. Use of flecainide acetate for the …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62135-660

What is NDC 62135-660?
62135-660 is the product NDC for Flecainide Acetate, Flecainide acetate 50 mg/1 tablet, 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?
Flecainide Acetate.
What is the active ingredient?
Flecainide acetate.
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 Flecainide Acetate?
55 other product NDCs are listed under this name. See all Flecainide Acetate 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 Flecainide Acetate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Flecainide AcetateFlecainide acetate 100 mg/1TabletOralUNICHEM PHARMACEUTICALS (USA), INC.76385-14676385-0146-0176385-0146-60
Flecainide AcetateFlecainide acetate 100 mg/1TabletOralBryant Ranch Prepack71335-257771335-2577-0171335-2577-0271335-2577-03+2 more
Flecainide AcetateFlecainide acetate 150 mg/1TabletOralUNICHEM PHARMACEUTICALS (USA), INC.76385-14776385-0147-0176385-0147-60
Flecainide AcetateFlecainide acetate 50 mg/1TabletOralUNICHEM PHARMACEUTICALS (USA), INC.76385-14576385-0145-0176385-0145-60
Flecainide AcetateFlecainide acetate 150 mg/1TabletOralBryant Ranch Prepack71335-265571335-2655-0171335-2655-0271335-2655-03+1 more
Flecainide AcetateFlecainide acetate 100 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-38372789-0383-0172789-0383-6072789-0383-93
Flecainide AcetateFlecainide acetate 150 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-38472789-0384-0172789-0384-6072789-0384-93
Flecainide AcetateFlecainide acetate 50 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-38572789-0385-0172789-0385-6072789-0385-93
Flecainide AcetateFlecainide acetate 100 mg/1TabletOralBryant Ranch Prepack71335-306371335-3063-0171335-3063-0271335-3063-03+2 more
Flecainide AcetateFlecainide acetate 50 mg/1TabletOralEpic Pharma, LLC42806-81742806-0817-01

All 56 Flecainide Acetate NDCs

Other NDCs under ANDA 079164

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

FDA NDC Directory listings under ANDA 079164
ProductStrengthForm · routeLabelerProduct NDC
Flecainide AcetateFlecainide acetate 150 mg/1TabletOralChartwell RX, LLC62135-662
Flecainide AcetateFlecainide acetate 100 mg/1TabletOralChartwell RX, LLC62135-661

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