What is NDC 0615-8246?

0615-8246 is the product NDC for Olanzapine, Olanzapine 20 mg/1 tablet, film coated, listed with the FDA by NCS HealthCare of KY, LLC dba Vangard Labs. It has 1 package NDC, shown above in 10- and 11-digit form.

NCS HealthCare of KY, LLC dba Vangard Labs, NDC labeler code 0615. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Olanzapine?

205 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Olanzapine NDC 0615-8246 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0615-8246Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00615-8246Add 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	Copy
0615-8246-39	00615824639	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8246-39)Marketed from Nov 2, 2018

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): Olanzapine
Generic name (nonproprietary): olanzapine
Active ingredients: Olanzapine — 20 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: NCS HealthCare of KY, LLC dba Vangard LabsNDC labeler code 0615
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202862
Marketing start: Aug 22, 2014
Listing expires: Dec 31, 2026
Identifiers: Product ID 0615-8246_23d2c50e-1be1-4357-bb2f-a9903ba4a43bSPL ID 23d2c50e-1be1-4357-bb2f-a9903ba4a43bSPL set ID 87b7fb23-c9b7-433f-bd17-cd3e91714c27RxCUI 200034, 283639, 312077, 312078, 314154UNII N7U69T4SZR
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

N400615824639 followed by a unit qualifier and the quantity

Package 00615-8246-39. 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 Mar 3, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Olanzapine is an atypical antipsychotic indicated: As oral formulation for the: · Treatment of schizophrenia. ( 1.1 ) · Adults: Efficacy was established in three clinical trials in patients with schizophrenia: two 6-week trials and one maintenance trial. ( 14.1 ) · Adolescents (ages 13-17): Efficacy was established in one 6-week trial in patients with schizophrenia ( 14.1 ). The increased potential (in adolescents compared with adults) for weight gain and dyslipidemia may lead clinicians to consider prescribing other drugs first in adolescents. ( 1.1 ) · Acute treatment of manic or mixed episodes associated with bipolar I disorder and maintenance treatment of bipolar I disorder. ( 1.2 ) · Ad…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0615-8246

What is NDC 0615-8246?: 0615-8246 is the product NDC for Olanzapine, Olanzapine 20 mg/1 tablet, film coated, listed with the FDA by NCS HealthCare of KY, LLC dba Vangard Labs. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Olanzapine.
What is the active ingredient?: Olanzapine.
Who is the labeler?: NCS HealthCare of KY, LLC dba Vangard Labs, NDC labeler code 0615. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Olanzapine?: 205 other product NDCs are listed under this name. See all Olanzapine 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 Olanzapine NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Olanzapine	Olanzapine 5 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0690	67046-0690-03
Olanzapine	Olanzapine 2.5 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4729	70518-4729-00
Olanzapine	Olanzapine 2.5 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-6693	55154-6693-00
olanzapine	Olanzapine 20 mg/1	Tablet, Orally disintegratingOral	Bionpharma Inc.	69452-564	69452-0564-13
olanzapine	Olanzapine 15 mg/1	Tablet, Orally disintegratingOral	Bionpharma Inc.	69452-563	69452-0563-13
olanzapine	Olanzapine 5 mg/1	Tablet, Orally disintegratingOral	Bionpharma Inc.	69452-561	69452-0561-13
olanzapine	Olanzapine 10 mg/1	Tablet, Orally disintegratingOral	Bionpharma Inc.	69452-562	69452-0562-13
Olanzapine	Olanzapine 10 mg/1	Tablet, Film coatedOral	Unit Dose Solutions, Inc.	87441-061	87441-0061-01
Olanzapine	Olanzapine 5 mg/1	Tablet, Film coatedOral	Unit Dose Solutions, Inc.	87441-062	87441-0062-01
Olanzapine	Olanzapine 20 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0072	67046-0072-03

All 206 Olanzapine NDCs

Other NDCs under ANDA 202862

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

FDA NDC Directory listings under ANDA 202862
Product	Strength	Form · route	Labeler	Product NDC
Olanzapine	Olanzapine 20 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-341
Olanzapine	Olanzapine 20 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-2337
Olanzapine	Olanzapine 10 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-364
Olanzapine	Olanzapine 15 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-2375
Olanzapine	Olanzapine 2.5 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-478
Olanzapine	Olanzapine 5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-0534
Olanzapine	Olanzapine 5 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0690
Olanzapine	Olanzapine 10 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-9661
Olanzapine	Olanzapine 15 mg/1	Tablet, Film coatedOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8566
Olanzapine	Olanzapine 5 mg/1	Tablet, Film coatedOral	Redpharm Drug	67296-2262
Olanzapine	Olanzapine 15 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-487
Olanzapine	Olanzapine 7.5 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-156
Olanzapine	Olanzapine 2.5 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-154
Olanzapine	Olanzapine 5 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-155
Olanzapine	Olanzapine 10 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-157
Olanzapine	Olanzapine 15 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-158
Olanzapine	Olanzapine 20 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-159
Olanzapine	Olanzapine 7.5 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1144
Olanzapine	Olanzapine 10 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	72162-2368
Olanzapine	Olanzapine 5 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-2698

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