olanzapine

Generic: olanzapine

Labeler: sandoz inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olanzapine
Generic Name olanzapine
Labeler sandoz inc
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR
Active Ingredients

olanzapine 10 mg/2mL

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 0781-3159
Product ID 0781-3159_b2fa51f4-e418-4113-bdd8-17f33ba250b7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201588
Listing Expiration 2026-12-31
Marketing Start 2011-10-24

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07813159
Hyphenated Format 0781-3159

Supplemental Identifiers

RxCUI
485968
UPC
0307813159728
UNII
N7U69T4SZR
NUI
N0000175430

Packaging Origin

Original Packager
true

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 ANDA201588 (source: ndc)
Routes
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 10 mg/2mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (0781-3159-72) / 2 mL in 1 VIAL
source: ndc

Packages (1)

0781-3159-72 1 VIAL in 1 CARTON (0781-3159-72) / 2 mL in 1 VIAL

Ingredients (1)

olanzapine (10 mg/2mL)

Linked Drug Pages (1)

Olanzapine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "b2fa51f4-e418-4113-bdd8-17f33ba250b7", "openfda": {"nui": ["N0000175430"], "upc": ["0307813159728"], "unii": ["N7U69T4SZR"], "rxcui": ["485968"], "spl_set_id": ["1e9666ef-4271-4834-8496-ccb3125d83db"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0781-3159-72)  / 2 mL in 1 VIAL", "package_ndc": "0781-3159-72", "marketing_start_date": "20111024"}], "brand_name": "Olanzapine", "product_id": "0781-3159_b2fa51f4-e418-4113-bdd8-17f33ba250b7", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0781-3159", "generic_name": "Olanzapine", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/2mL"}], "application_number": "ANDA201588", "marketing_category": "ANDA", "marketing_start_date": "20111024", "listing_expiration_date": "20261231"}