Package 71335-2627-3

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 71335-2627-3
Digits Only 7133526273
Product NDC 71335-2627
Description

90 TABLET, FILM COATED in 1 BOTTLE (71335-2627-3)

Marketing

Marketing Status
Marketed Since 2025-06-02
Brand olanzapine
Generic olanzapine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bdb8dfd3-6c84-491b-962b-becf607b42f0", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["314154"], "spl_set_id": ["3c9963b1-c498-48a0-a3a1-1eaa6a1028fc"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2627-1)", "package_ndc": "71335-2627-1", "marketing_start_date": "20250602"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2627-2)", "package_ndc": "71335-2627-2", "marketing_start_date": "20250602"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2627-3)", "package_ndc": "71335-2627-3", "marketing_start_date": "20250602"}], "brand_name": "Olanzapine", "product_id": "71335-2627_bdb8dfd3-6c84-491b-962b-becf607b42f0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "71335-2627", "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": "ANDA076255", "marketing_category": "ANDA", "marketing_start_date": "20131210", "listing_expiration_date": "20261231"}