Package 55111-168-01

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 55111-168-01
Digits Only 5511116801
Product NDC 55111-168
Description

100 TABLET, FILM COATED in 1 BOTTLE (55111-168-01)

Marketing

Marketing Status
Marketed Since 2012-04-23
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": "e0d25a13-d2e2-0299-98bb-4d523d75cb76", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["283639", "312077"], "spl_set_id": ["a4c525da-c2f6-b804-af49-601295922254"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Dr. Reddy's Laboratories Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (55111-168-01)", "package_ndc": "55111-168-01", "marketing_start_date": "20120423"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (55111-168-05)", "package_ndc": "55111-168-05", "marketing_start_date": "20120423"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (55111-168-30)", "package_ndc": "55111-168-30", "marketing_start_date": "20120423"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (55111-168-60)", "package_ndc": "55111-168-60", "marketing_start_date": "20120423"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-168-78)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-168-79)", "package_ndc": "55111-168-78", "marketing_start_date": "20120423"}], "brand_name": "Olanzapine", "product_id": "55111-168_e0d25a13-d2e2-0299-98bb-4d523d75cb76", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "55111-168", "generic_name": "Olanzapine", "labeler_name": "Dr. Reddy's Laboratories Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "20 mg/1"}], "application_number": "ANDA076133", "marketing_category": "ANDA", "marketing_start_date": "20120423", "listing_expiration_date": "20261231"}