olanzapine

Generic: olanzapine

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olanzapine
Generic Name olanzapine
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

olanzapine 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1936
Product ID 71335-1936_d9e3e5fe-a131-436f-a89d-18056479a83f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202050
Listing Expiration 2026-12-31
Marketing Start 2012-04-23

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351936
Hyphenated Format 71335-1936

Supplemental Identifiers

RxCUI
314154
UNII
N7U69T4SZR
NUI
N0000175430

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name olanzapine (source: ndc)
Generic Name olanzapine (source: ndc)
Application Number ANDA202050 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1936-1)
  • 60 TABLET in 1 BOTTLE (71335-1936-2)
  • 90 TABLET in 1 BOTTLE (71335-1936-3)
source: ndc

Packages (3)

71335-1936-1 30 TABLET in 1 BOTTLE (71335-1936-1) 71335-1936-2 60 TABLET in 1 BOTTLE (71335-1936-2) 71335-1936-3 90 TABLET in 1 BOTTLE (71335-1936-3)

Ingredients (1)

olanzapine (10 mg/1)

Linked Drug Pages (1)

Olanzapine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d9e3e5fe-a131-436f-a89d-18056479a83f", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["314154"], "spl_set_id": ["4e90e30c-78a1-486f-a13c-f1ff798216be"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1936-1)", "package_ndc": "71335-1936-1", "marketing_start_date": "20240718"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1936-2)", "package_ndc": "71335-1936-2", "marketing_start_date": "20240718"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1936-3)", "package_ndc": "71335-1936-3", "marketing_start_date": "20240718"}], "brand_name": "Olanzapine", "product_id": "71335-1936_d9e3e5fe-a131-436f-a89d-18056479a83f", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "71335-1936", "generic_name": "Olanzapine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/1"}], "application_number": "ANDA202050", "marketing_category": "ANDA", "marketing_start_date": "20120423", "listing_expiration_date": "20261231"}