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, ORALLY DISINTEGRATING
Routes
ORAL
Active Ingredients

olanzapine 15 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-8714
Product ID 63629-8714_33629b13-1f42-05cd-e063-6294a90ada76
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091265
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 636298714
Hyphenated Format 63629-8714

Supplemental Identifiers

RxCUI
351107
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 ANDA091265 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63629-8714-1)
source: ndc

Packages (1)

Ingredients (1)

olanzapine (15 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "33629b13-1f42-05cd-e063-6294a90ada76", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["351107"], "spl_set_id": ["d5a9f78e-56f4-4249-800c-5f52a99fa84b"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63629-8714-1)", "package_ndc": "63629-8714-1", "marketing_start_date": "20111024"}], "brand_name": "Olanzapine", "product_id": "63629-8714_33629b13-1f42-05cd-e063-6294a90ada76", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "63629-8714", "generic_name": "Olanzapine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "15 mg/1"}], "application_number": "ANDA091265", "marketing_category": "ANDA", "marketing_start_date": "20111024", "listing_expiration_date": "20261231"}