NDC 0093-5771

Olanzapine

Olanzapine

Olanzapine is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Teva Pharmaceuticals Usa, Inc.. The primary component is Olanzapine.

• Product ID: 0093-5771_30a50dd0-2f19-40af-9bd5-c26ad58497ab
• NDC: 0093-5771
• Product Type: Human Prescription Drug
• Proprietary Name: Olanzapine
• Generic Name: Olanzapine
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2011-10-24
• Marketing Category: ANDA / ANDA
• Application Number: ANDA076000
• Labeler Name: Teva Pharmaceuticals USA, Inc.
• Substance Name: OLANZAPINE
• Active Ingredient Strength: 15 mg/1
• Pharm Classes: Atypical Antipsychotic [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0093-5771-56

30 TABLET, FILM COATED in 1 BOTTLE (0093-5771-56)

• Marketing Start Date: 2011-10-24
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0093-5771-01 [00093577101]

Olanzapine TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA076000
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2011-10-24
• Marketing End Date: 2017-10-31

NDC 0093-5771-56 [00093577156]

Olanzapine TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA076000
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2011-10-24
• Marketing End Date: 2018-09-30

NDC 0093-5771-10 [00093577110]

Olanzapine TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA076000
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2011-10-24
• Marketing End Date: 2018-03-31

Drug Details

Active Ingredients

Ingredient	Strength
OLANZAPINE	15 mg/1

OpenFDA Data

• SPL SET ID: f6ec3e3e-24c3-4360-b712-ca6017af1347
• Manufacturer:
  • Teva Pharmaceuticals USA, Inc.
• UNII:
  • N7U69T4SZR
• RxNorm Concept Unique ID - RxCUI:
  • 312079
  • 200034
  • 314154
  • 312077
  • 312078
• UPC Code:
  • 0300935768564
  • 0300935770567
  • 0300935769561
  • 0300935771564
  • 0300935767567

Pharmacological Class

• Atypical Antipsychotic [EPC]

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

NDC	Brand Name	Generic Name
67877-175	Olanzapine	Olanzapine
67877-174	Olanzapine	Olanzapine
67877-172	Olanzapine	Olanzapine
67877-173	Olanzapine	Olanzapine
67877-176	Olanzapine	Olanzapine
67877-177	Olanzapine	Olanzapine
68084-529	Olanzapine	Olanzapine
68084-723	Olanzapine	Olanzapine
68084-528	Olanzapine	Olanzapine
68084-740	Olanzapine	Olanzapine
68084-525	Olanzapine	Olanzapine
68258-7095	Olanzapine	Olanzapine
68258-7152	Olanzapine	Olanzapine
68258-7153	Olanzapine	Olanzapine
68258-7154	Olanzapine	Olanzapine
68382-365	olanzapine	olanzapine
68382-368	olanzapine	olanzapine
68258-7096	Olanzapine	Olanzapine
68382-367	olanzapine	olanzapine
68382-364	olanzapine	olanzapine
68382-366	olanzapine	olanzapine
68382-369	olanzapine	olanzapine
68788-7161	Olanzapine	Olanzapine
0517-0955	Olanzapine	Olanzapine
69189-5510	Olanzapine	Olanzapine
69543-384	Olanzapine	Olanzapine
69543-380	Olanzapine	Olanzapine
69543-381	Olanzapine	Olanzapine
69543-383	Olanzapine	Olanzapine
69543-382	Olanzapine	Olanzapine
69543-385	Olanzapine	Olanzapine
69807-2012	Olanzapine	Olanzapine
69807-2011	Olanzapine	Olanzapine
69807-2013	Olanzapine	Olanzapine
70518-0026	Olanzapine	Olanzapine
70518-0148	Olanzapine	Olanzapine
70518-0145	Olanzapine	Olanzapine
70518-0149	Olanzapine	Olanzapine
70518-0314	Olanzapine	Olanzapine
70518-0477	Olanzapine	Olanzapine
70518-0110	Olanzapine	Olanzapine
70518-0616	Olanzapine	Olanzapine
70518-0144	Olanzapine	Olanzapine
70518-0433	Olanzapine	Olanzapine
70518-1206	Olanzapine	Olanzapine
70518-0921	Olanzapine	Olanzapine
70518-1207	Olanzapine	Olanzapine
70518-0615	Olanzapine	Olanzapine
70518-1115	Olanzapine	Olanzapine
70518-1154	Olanzapine	Olanzapine