NDC codes

FDA NDC Directory
Product NDC (as listed)59651-723Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59651-0723Add 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
59651-723-015965107230159651072301100 TABLET in 1 BOTTLE (59651-723-01)Marketed from Jan 17, 2023
59651-723-9959651072399596510723991000 TABLET in 1 BOTTLE (59651-723-99)Marketed from Jan 17, 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)
Clonazepam
Generic name (nonproprietary)
clonazepam
Active ingredients
Clonazepam — 1 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Aurobindo Pharma LimitedNDC labeler code 59651
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075150
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 59651-723_b1582eb7-af35-45d5-a52e-0e380d08527dSPL ID b1582eb7-af35-45d5-a52e-0e380d08527dSPL set ID b1582eb7-af35-45d5-a52e-0e380d08527dRxCUI 197527, 197528, 197529UNII 5PE9FDE8GB
Pharmacologic class
Benzodiazepine

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

N459651072301 followed by a unit qualifier and the quantity

Package 59651-0723-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Seizure Disorders: Clonazepam tablets are useful alone or as an adjunct in the treatment of the Lennox-Gastaut syndrome (petit mal variant), akinetic, and myoclonic seizures. In patients with absence seizures (petit mal) who have failed to respond to succinimides, clonazepam tablets may be useful. Some loss of effect may occur during the course of clonazepam treatment (see PRECAUTIONS: Loss of Effect ). Panic Disorder: Clonazepam tablets are indicated for the treatment of panic disorder, with or without agoraphobia, as defined in DSM-V. Panic disorder is characterized by the occurrence of unexpected panic attacks and associated concern about having additional attacks, w…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59651-723

What is NDC 59651-723?
59651-723 is the product NDC for Clonazepam, Clonazepam 1 mg/1 tablet, listed with the FDA by Aurobindo Pharma Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Clonazepam.
What is the active ingredient?
Clonazepam.
Who is the labeler?
Aurobindo Pharma Limited, NDC labeler code 59651. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Clonazepam?
141 other product NDCs are listed under this name. See all Clonazepam 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 Clonazepam NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ClonazepamClonazepam 2 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-878168788-8781-0268788-8781-0368788-8781-06+1 more
ClonazepamClonazepam .5 mg/1TabletOralUnit Dose Solutions, Inc.87441-09087441-0090-01
ClonazepamClonazepam .25 mg/1TabletOralTruPharma LLC52817-30552817-0305-90
ClonazepamClonazepam 1 mg/1TabletOralCoupler LLC67046-049367046-0493-03
ClonazepamClonazepam .5 mg/1TabletOralUnit Dose Solutions, Inc.87441-02187441-0021-01
ClonazepamClonazepam 1 mg/1TabletOralUnit Dose Solutions, Inc.87441-02287441-0022-01
ClonazepamClonazepam .25 mg/1TabletOralAdvagen Pharma Ltd72888-49772888-0497-0172888-0497-0272888-0497-03+1 more
clonazepamClonazepam 1 mg/1Tablet, Orally disintegratingOralAdvagen Pharma Ltd72888-13672888-0136-2972888-0136-31
clonazepamClonazepam .125 mg/1Tablet, Orally disintegratingOralAdvagen Pharma Ltd72888-13372888-0133-2972888-0133-31
clonazepamClonazepam .25 mg/1Tablet, Orally disintegratingOralAdvagen Pharma Ltd72888-13472888-0134-2972888-0134-31

All 142 Clonazepam NDCs

Other NDCs under ANDA 075150

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

FDA NDC Directory listings under ANDA 075150
ProductStrengthForm · routeLabelerProduct NDC
ClonazepamClonazepam .5 mg/1TabletOralAurobindo Pharma Limited59651-722
ClonazepamClonazepam 2 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8781
ClonazepamClonazepam 2 mg/1TabletOralREMEDYREPACK INC.70518-3849
ClonazepamClonazepam .5 mg/1TabletOralREMEDYREPACK INC.70518-3960
ClonazepamClonazepam 1 mg/1TabletOralREMEDYREPACK INC.70518-4074
ClonazepamClonazepam 2 mg/1TabletOralBryant Ranch Prepack71335-2653
ClonazepamClonazepam 1 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-852
ClonazepamClonazepam .5 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-855
ClonazepamClonazepam 1 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0357
ClonazepamClonazepam .5 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0402
ClonazepamClonazepam 1 mg/1TabletOralProficient Rx LP82804-272

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