What is NDC 71335-2599?

71335-2599 is the product NDC for Olanzapine, Olanzapine 5 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 5 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 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 71335-2599 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2599Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2599Add 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
71335-2599-1	7133525990171335259901	30 TABLET, FILM COATED in 1 BOTTLE (71335-2599-1)Marketed from Jun 5, 2025
71335-2599-2	7133525990271335259902	15 TABLET, FILM COATED in 1 BOTTLE (71335-2599-2)Marketed from Jun 5, 2025
71335-2599-3	7133525990371335259903	60 TABLET, FILM COATED in 1 BOTTLE (71335-2599-3)Marketed from Jun 5, 2025
71335-2599-4	7133525990471335259904	90 TABLET, FILM COATED in 1 BOTTLE (71335-2599-4)Marketed from Jun 5, 2025
71335-2599-5	7133525990571335259905	120 TABLET, FILM COATED in 1 BOTTLE (71335-2599-5)Marketed from Jun 5, 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): Olanzapine
Generic name (nonproprietary): olanzapine
Active ingredients: Olanzapine — 5 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090798
Marketing start: Apr 23, 2012
Listing expires: Dec 31, 2026
Identifiers: Product ID 71335-2599_2b67795f-346b-4d05-9089-b0dd16244e07SPL ID 2b67795f-346b-4d05-9089-b0dd16244e07SPL set ID 1866a03c-eac9-44a1-8f33-7dc6e8a8c06aRxCUI 312078UNII 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

N471335259901 followed by a unit qualifier and the quantity

Package 71335-2599-01. 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 5, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Olanzapine tablets are 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 to 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 …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2599

What is NDC 71335-2599?: 71335-2599 is the product NDC for Olanzapine, Olanzapine 5 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 5 package NDCs, 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?: 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 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 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 20 mg/1	Tablet, Orally disintegratingOral	Bionpharma Inc.	69452-564	69452-0564-13
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 090798

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

FDA NDC Directory listings under ANDA 090798
Product	Strength	Form · route	Labeler	Product NDC
Olanzapine	Olanzapine 2.5 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-6693
Olanzapine	Olanzapine 2.5 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	60429-620
Olanzapine	Olanzapine 5 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	60429-621
Olanzapine	Olanzapine 7.5 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	60429-622
Olanzapine	Olanzapine 10 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	60429-623
Olanzapine	Olanzapine 15 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	60429-624
Olanzapine	Olanzapine 20 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	60429-625
Olanzapine	Olanzapine 2.5 mg/1	Tablet, Film coatedOral	Apotex Corp.	60505-3110
Olanzapine	Olanzapine 5 mg/1	Tablet, Film coatedOral	Apotex Corp.	60505-3111
Olanzapine	Olanzapine 7.5 mg/1	Tablet, Film coatedOral	Apotex Corp.	60505-3112
Olanzapine	Olanzapine 10 mg/1	Tablet, Film coatedOral	Apotex Corp.	60505-3113
Olanzapine	Olanzapine 15 mg/1	Tablet, Film coatedOral	Apotex Corp.	60505-3114
Olanzapine	Olanzapine 20 mg/1	Tablet, Film coatedOral	Apotex Corp.	60505-3140
Olanzapine	Olanzapine 10 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-429
Olanzapine	Olanzapine 2.5 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-453
Olanzapine	Olanzapine 5 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-844
Olanzapine	Olanzapine 5 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-0314
Olanzapine	Olanzapine 2.5 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-3568
Olanzapine	Olanzapine 15 mg/1	Tablet, Film coatedOral	Aphena Pharma Solutions - Tennessee, LLC	71610-419
Olanzapine	Olanzapine 20 mg/1	Tablet, Film coatedOral	Proficient Rx LP	82804-067