olanzapine

Generic: olanzapine

Labeler: golden state medical supply, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olanzapine
Generic Name olanzapine
Labeler golden state medical supply, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

olanzapine 5 mg/1

Manufacturer
Golden State Medical Supply, Inc.

Identifiers & Regulatory

Product NDC 60429-621
Product ID 60429-621_338a0fc3-780f-e692-e063-6394a90a3155
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090798
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 60429621
Hyphenated Format 60429-621

Supplemental Identifiers

RxCUI
200034 283639 312077 312078 312079 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 ANDA090798 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (60429-621-01)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (60429-621-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (60429-621-30)
source: ndc

Packages (3)

60429-621-01 100 TABLET, FILM COATED in 1 BOTTLE (60429-621-01) 60429-621-10 1000 TABLET, FILM COATED in 1 BOTTLE (60429-621-10) 60429-621-30 30 TABLET, FILM COATED in 1 BOTTLE (60429-621-30)

Ingredients (1)

olanzapine (5 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": "338a0fc3-780f-e692-e063-6394a90a3155", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["200034", "283639", "312077", "312078", "312079", "314154"], "spl_set_id": ["a1dfb4e7-4143-4422-b7a7-292e4fd75044"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (60429-621-01)", "package_ndc": "60429-621-01", "marketing_start_date": "20250423"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (60429-621-10)", "package_ndc": "60429-621-10", "marketing_start_date": "20191016"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (60429-621-30)", "package_ndc": "60429-621-30", "marketing_start_date": "20191016"}], "brand_name": "Olanzapine", "product_id": "60429-621_338a0fc3-780f-e692-e063-6394a90a3155", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "60429-621", "generic_name": "Olanzapine", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "5 mg/1"}], "application_number": "ANDA090798", "marketing_category": "ANDA", "marketing_start_date": "20120423", "listing_expiration_date": "20261231"}