NDC codes

FDA NDC Directory
Product NDC (as listed)0093-3212Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00093-3212Add 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
0093-3212-0100093321201100 TABLET in 1 BOTTLE (0093-3212-01)Marketed from Sep 17, 1996
0093-3212-0500093321205500 TABLET in 1 BOTTLE (0093-3212-05)Marketed from Aug 21, 1998

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 074569
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 0093-3212_d6abe4e3-7699-4ead-95f4-739a961b23adSPL ID d6abe4e3-7699-4ead-95f4-739a961b23adSPL set ID 8069b1a0-7c06-4252-b44e-e2eef065d9b8RxCUI 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

N400093321201 followed by a unit qualifier and the quantity

Package 00093-3212-01. 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, …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 074569

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

FDA NDC Directory listings under ANDA 074569
ProductStrengthForm · routeLabelerProduct NDC
ClonazepamClonazepam .5 mg/1TabletOralProficient Rx LP63187-226
ClonazepamClonazepam 1 mg/1TabletOralCoupler LLC67046-0493
ClonazepamClonazepam .5 mg/1TabletOralA-S Medication Solutions50090-4841
ClonazepamClonazepam .5 mg/1TabletOralREMEDYREPACK INC.70518-2507
ClonazepamClonazepam .5 mg/1TabletOralClinical Solutions Wholesale, LLC58118-0832
ClonazepamClonazepam 1 mg/1TabletOralREMEDYREPACK INC.70518-3144
ClonazepamClonazepam .5 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC67544-529
ClonazepamClonazepam .5 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0093-0832
ClonazepamClonazepam 2 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0093-3213
ClonazepamClonazepam 2 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-749

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