What is NDC 71335-2653?

71335-2653 is the product NDC for Clonazepam, Clonazepam 2 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 6 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Clonazepam NDC 71335-2653 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2653Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2653Add 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
71335-2653-1	7133526530171335265301	30 TABLET in 1 BOTTLE (71335-2653-1)Marketed from Jun 20, 2025
71335-2653-2	7133526530271335265302	60 TABLET in 1 BOTTLE (71335-2653-2)Marketed from Jun 20, 2025
71335-2653-3	7133526530371335265303	90 TABLET in 1 BOTTLE (71335-2653-3)Marketed from Jun 20, 2025
71335-2653-4	7133526530471335265304	120 TABLET in 1 BOTTLE (71335-2653-4)Marketed from Jun 20, 2025
71335-2653-5	7133526530571335265305	10 TABLET in 1 BOTTLE (71335-2653-5)Marketed from Jun 20, 2025
71335-2653-6	7133526530671335265306	180 TABLET in 1 BOTTLE (71335-2653-6)Marketed from Jun 20, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 2 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075150
Marketing start: Jan 17, 2023
Listing expires: Dec 31, 2026
DEA schedule: CIV
Other FDA classes: Benzodiazepines (Chemical structure)
Identifiers: Product ID 71335-2653_109c2b88-9bf1-4537-aab1-16e804fcb49aSPL ID 109c2b88-9bf1-4537-aab1-16e804fcb49aSPL set ID dec8b5b2-2490-4880-a8d1-707b57954297RxCUI 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

N471335265301 followed by a unit qualifier and the quantity

Package 71335-2653-01. 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 Jun 20, 2025. 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 71335-2653

What is NDC 71335-2653?: 71335-2653 is the product NDC for Clonazepam, Clonazepam 2 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 6 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?: Bryant Ranch Prepack, NDC labeler code 71335. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Clonazepam	Clonazepam 2 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8781	68788-8781-0268788-8781-0368788-8781-06+1 more
Clonazepam	Clonazepam .5 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-090	87441-0090-01
Clonazepam	Clonazepam .25 mg/1	TabletOral	TruPharma LLC	52817-305	52817-0305-90
Clonazepam	Clonazepam 1 mg/1	TabletOral	Coupler LLC	67046-0493	67046-0493-03
Clonazepam	Clonazepam .5 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-021	87441-0021-01
Clonazepam	Clonazepam 1 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-022	87441-0022-01
Clonazepam	Clonazepam .25 mg/1	TabletOral	Advagen Pharma Ltd	72888-497	72888-0497-0172888-0497-0272888-0497-03+1 more
clonazepam	Clonazepam 1 mg/1	Tablet, Orally disintegratingOral	Advagen Pharma Ltd	72888-136	72888-0136-2972888-0136-31
clonazepam	Clonazepam .125 mg/1	Tablet, Orally disintegratingOral	Advagen Pharma Ltd	72888-133	72888-0133-2972888-0133-31
clonazepam	Clonazepam .25 mg/1	Tablet, Orally disintegratingOral	Advagen Pharma Ltd	72888-134	72888-0134-2972888-0134-31

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
Product	Strength	Form · route	Labeler	Product NDC
Clonazepam	Clonazepam .5 mg/1	TabletOral	Aurobindo Pharma Limited	59651-722
Clonazepam	Clonazepam 1 mg/1	TabletOral	Aurobindo Pharma Limited	59651-723
Clonazepam	Clonazepam 2 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8781
Clonazepam	Clonazepam 2 mg/1	TabletOral	REMEDYREPACK INC.	70518-3849
Clonazepam	Clonazepam .5 mg/1	TabletOral	REMEDYREPACK INC.	70518-3960
Clonazepam	Clonazepam 1 mg/1	TabletOral	REMEDYREPACK INC.	70518-4074
Clonazepam	Clonazepam 1 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-852
Clonazepam	Clonazepam .5 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-855
Clonazepam	Clonazepam 1 mg/1	TabletOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0357
Clonazepam	Clonazepam .5 mg/1	TabletOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0402
Clonazepam	Clonazepam 1 mg/1	TabletOral	Proficient Rx LP	82804-272