Package 13668-170-05

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 13668-170-05
Digits Only 1366817005
Product NDC 13668-170
Description

500 TABLET in 1 BOTTLE (13668-170-05)

Marketing

Marketing Status
Marketed Since 2026-02-28
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": "1a64829a-2434-4c8d-8e58-9b28758e4b88", "openfda": {"nui": ["N0000175430"], "upc": ["0313668088304", "0313668170306", "0313668169300", "0313668171303", "0313668168303", "0313668166309", "0313668090307", "0313668089301", "0313668167306", "0313668086300"], "unii": ["N7U69T4SZR"], "rxcui": ["200034", "283639", "312076", "312077", "312078", "312079", "314154", "314155", "351107", "351108"], "spl_set_id": ["2cb1bebe-0ced-46d8-bf21-c28a9acc4a15"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (13668-170-01)", "package_ndc": "13668-170-01", "marketing_start_date": "20260228"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (13668-170-05)", "package_ndc": "13668-170-05", "marketing_start_date": "20260228"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (13668-170-10)", "package_ndc": "13668-170-10", "marketing_start_date": "20260228"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (13668-170-30)", "package_ndc": "13668-170-30", "marketing_start_date": "20260228"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (13668-170-60)", "package_ndc": "13668-170-60", "marketing_start_date": "20260228"}], "brand_name": "OLANZAPINE", "product_id": "13668-170_1a64829a-2434-4c8d-8e58-9b28758e4b88", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "13668-170", "generic_name": "OLANZAPINE", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLANZAPINE", "active_ingredients": [{"name": "OLANZAPINE", "strength": "15 mg/1"}], "application_number": "ANDA091434", "marketing_category": "ANDA", "marketing_start_date": "20260228", "listing_expiration_date": "20271231"}