Package 0832-6081-03

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 0832-6081-03
Digits Only 0832608103
Product NDC 0832-6081
Product ID 0832-6081_8360dfb0-5f3a-4b86-8b46-fc89c12aad6b
Description

30 TABLET in 1 BOTTLE (0832-6081-03)

Marketing

Marketing Status
Discontinued 2026-08-31
Brand olanzapine
Generic olanzapine
Sample Package No

Linked Drug Pages (1)

Olanzapine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8360dfb0-5f3a-4b86-8b46-fc89c12aad6b", "openfda": {"nui": ["N0000175430"], "upc": ["0308326078032", "0308326082039", "0308326081032", "0308326079039", "0308326083036", "0308326080035"], "unii": ["N7U69T4SZR"], "rxcui": ["200034", "283639", "312077", "312078", "312079", "314154"], "spl_set_id": ["dbe23f33-9e7d-49a7-8528-fa290661a96f"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (0832-6081-03)", "package_ndc": "0832-6081-03", "marketing_end_date": "20260831", "marketing_start_date": "20240815"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0832-6081-50)", "package_ndc": "0832-6081-50", "marketing_end_date": "20260831", "marketing_start_date": "20240815"}], "brand_name": "Olanzapine", "product_id": "0832-6081_8360dfb0-5f3a-4b86-8b46-fc89c12aad6b", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0832-6081", "generic_name": "Olanzapine", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/1"}], "application_number": "ANDA204319", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20160127"}