olanzapine

Generic: olanzapine

Labeler: cardinal health 107, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olanzapine
Generic Name olanzapine
Labeler cardinal health 107, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

olanzapine 10 mg/1

Manufacturer
Cardinal Health 107, LLC

Identifiers & Regulatory

Product NDC 55154-6889
Product ID 55154-6889_ce9eff03-1df5-4804-97e9-800aa0d5e22e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076255
Listing Expiration 2027-12-31
Marketing Start 2012-04-23

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 551546889
Hyphenated Format 55154-6889

Supplemental Identifiers

RxCUI
312078 314154
UPC
0055154688109 0055154688901
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 ANDA076255 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BAG (55154-6889-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

olanzapine (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ce9eff03-1df5-4804-97e9-800aa0d5e22e", "openfda": {"nui": ["N0000175430"], "upc": ["0055154688109", "0055154688901"], "unii": ["N7U69T4SZR"], "rxcui": ["312078", "314154"], "spl_set_id": ["38a89689-efc2-4931-8f65-868dc0248d6a"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-6889-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-6889-0", "marketing_start_date": "20120423"}], "brand_name": "Olanzapine", "product_id": "55154-6889_ce9eff03-1df5-4804-97e9-800aa0d5e22e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "55154-6889", "generic_name": "Olanzapine", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/1"}], "application_number": "ANDA076255", "marketing_category": "ANDA", "marketing_start_date": "20120423", "listing_expiration_date": "20271231"}