NDC codes

FDA NDC Directory
Product NDC (as listed)0093-5377Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00093-5377Add 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
0093-5377-010009353770100093537701100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (0093-5377-01)Marketed from Jul 30, 2020
0093-5377-84000935377840009353778448 BLISTER PACK in 1 CARTON (0093-5377-84) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0093-5377-19)Marketed from Jul 30, 2020

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)
Clozapine
Generic name (nonproprietary)
clozapine
Active ingredients
Clozapine — 200 mg/1
Dosage form
Tablet, Orally disintegrating
Route
Oral
Labeler
Teva Pharmaceuticals USA, Inc.NDC labeler code 0093
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090308
Marketing start
Listing expires
Identifiers
Product ID 0093-5377_1b735bc2-6341-40af-8696-e61621d91ee8SPL ID 1b735bc2-6341-40af-8696-e61621d91ee8SPL set ID 6fccf4f7-2e30-4272-9800-225aaef20584RxCUI 476177, 476179, 721773, 996921, 1006801UNII J60AR2IKIC
Pharmacologic class
Atypical Antipsychotic

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

N400093537701 followed by a unit qualifier and the quantity

Package 00093-5377-01. 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)

Clozapine orally disintegrating tablets (Clozapine ODT) is an atypical antipsychotic indicated for: Treatment of severely ill patients with schizophrenia who fail to respond adequately to standard antipsychotic treatment. Because of the risks of severe neutropenia and of seizure associated with its use, Clozapine ODT should be used only in patients who have failed to respond adequately to standard antipsychotic treatment ( 1.1 ) Reducing the risk of recurrent suicidal behavior in patients with schizophrenia or schizoaffective disorder who are judged to be at chronic risk for re-experiencing suicidal behavior ( 1.2 ) 1.1 Treatment-resistant Schizophrenia Clozapine Orally Disintegrating Tablet…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0093-5377

What is NDC 0093-5377?
0093-5377 is the product NDC for Clozapine, Clozapine 200 mg/1 tablet, orally disintegrating, listed with the FDA by Teva Pharmaceuticals USA, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Clozapine.
What is the active ingredient?
Clozapine.
Who is the labeler?
Teva Pharmaceuticals USA, Inc., NDC labeler code 0093. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Clozapine?
43 other product NDCs are listed under this name. See all Clozapine 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 Clozapine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ClozapineClozapine 25 mg/1TabletOralNorthStar Rx LLC72603-91172603-0911-01
ClozapineClozapine 50 mg/1TabletOralNorthStar Rx LLC72603-91272603-0912-01
ClozapineClozapine 100 mg/1TabletOralNorthStar Rx LLC72603-91372603-0913-0172603-0913-02
ClozapineClozapine 200 mg/1TabletOralNorthStar Rx LLC72603-91472603-0914-01
ClozapineClozapine 100 mg/1Tablet, Orally disintegratingOralSafecor Health, LLC48433-02248433-0022-04
ClozapineClozapine 25 mg/1TabletOralSafecor Health LLC48433-02348433-0023-20
ClozapineClozapine 100 mg/1TabletOralSafecor Health LLC48433-02448433-0024-20
ClozapineClozapine 200 mg/1TabletOralSafecor Health LLC48433-02548433-0025-20
ClozapineClozapine 12.5 mg/1Tablet, Orally disintegratingOralAurobindo Pharma Limited59651-26059651-0260-01
ClozapineClozapine 25 mg/1Tablet, Orally disintegratingOralAurobindo Pharma Limited59651-26159651-0261-0159651-0261-48

All 44 Clozapine NDCs

Other NDCs under ANDA 090308

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

FDA NDC Directory listings under ANDA 090308
ProductStrengthForm · routeLabelerProduct NDC
ClozapineClozapine 150 mg/1Tablet, Orally disintegratingOralTeva Pharmaceuticals USA, Inc.0093-5376
ClozapineClozapine 12.5 mg/1Tablet, Orally disintegratingOralTeva Pharmaceuticals USA, Inc.0093-5416
ClozapineClozapine 25 mg/1Tablet, Orally disintegratingOralTeva Pharmaceuticals USA, Inc.0093-5417
ClozapineClozapine 100 mg/1Tablet, Orally disintegratingOralTeva Pharmaceuticals USA, Inc.0093-5419

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