NDC 0002-4415

Zyprexa

Olanzapine

Zyprexa is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Eli Lilly And Company. The primary component is Olanzapine.

• Product ID: 0002-4415_7184cd07-6f72-4413-9d11-daa74ef14b03
• NDC: 0002-4415
• Product Type: Human Prescription Drug
• Proprietary Name: Zyprexa
• Generic Name: Olanzapine
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2000-01-10
• Marketing Category: NDA / NDA
• Application Number: NDA020592
• Labeler Name: Eli Lilly and Company
• Substance Name: OLANZAPINE
• Active Ingredient Strength: 15 mg/1
• Pharm Classes: Atypical Antipsychotic [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 0002-4415-30

30 TABLET in 1 BOTTLE (0002-4415-30)

• Marketing Start Date: 2000-01-10
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0002-4415-04 [00002441504]

Zyprexa TABLET

• Marketing Category: NDA
• Application Number: NDA020592
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2000-01-10
• Marketing End Date: 2014-10-15

NDC 0002-4415-01 [00002441501]

Zyprexa TABLET

• Marketing Category: NDA
• Application Number: NDA020592
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2000-01-10
• Marketing End Date: 2014-10-15

NDC 0002-4415-33 [00002441533]

Zyprexa TABLET

• Marketing Category: NDA
• Application Number: NDA020592
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2000-01-10
• Marketing End Date: 2014-10-15

NDC 0002-4415-30 [00002441530]

Zyprexa TABLET

• Marketing Category: NDA
• Application Number: NDA020592
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2000-01-10

NDC 0002-4415-07 [00002441507]

Zyprexa TABLET

• Marketing Category: NDA
• Application Number: NDA020592
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2000-01-10
• Marketing End Date: 2013-08-06

Drug Details

Active Ingredients

Ingredient	Strength
OLANZAPINE	15 mg/1

OpenFDA Data

• SPL SET ID: d5051fbc-846b-4946-82df-341fb1216341
• Manufacturer:
  • Eli Lilly and Company
• UNII:
  • N7U69T4SZR
• RxNorm Concept Unique ID - RxCUI:
  • 200034
  • 212405
  • 351108
  • 283639
  • 485968
  • 351107
  • 754506
  • 754505
  • 754504
  • 754503
  • 284514
  • 312077
  • 312076
  • 312079
  • 312078
  • 545353
  • 261337
  • 314154
  • 314155
  • 153047
  • 153046
  • 153048
• UPC Code:
  • 0300024420304
  • 0300024117303
  • 0300024415300
  • 0300024112308
  • 0300024115309
  • 0300024116306

Pharmacological Class

• Atypical Antipsychotic [EPC]

NDC Crossover Matching brand name "Zyprexa" or generic name "Olanzapine"

NDC	Brand Name	Generic Name
0002-4112	Zyprexa	Olanzapine
0002-4115	Zyprexa	Olanzapine
0002-4116	Zyprexa	Olanzapine
0002-4117	Zyprexa	Olanzapine
0002-4415	Zyprexa	Olanzapine
0002-4420	Zyprexa	Olanzapine
0002-4453	ZYPREXA	Olanzapine
0002-4454	ZYPREXA	Olanzapine
0002-4455	ZYPREXA	Olanzapine
68258-7092	Zyprexa	Zyprexa
68258-7093	Zyprexa	Zyprexa
68258-7090	Zyprexa	Zyprexa
68258-7091	Zyprexa	Zyprexa
70518-1465	Zyprexa	Zyprexa
21695-144	Zyprexa	Zyprexa
21695-140	Zyprexa	Zyprexa
21695-142	Zyprexa	Zyprexa
49999-606	Zyprexa	Zyprexa
52959-579	Zyprexa	Zyprexa
55289-213	Zyprexa	Zyprexa