Package 55111-163-30

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 55111-163-30
Digits Only 5511116330
Product NDC 55111-163
Description

30 TABLET, FILM COATED in 1 BOTTLE (55111-163-30)

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": "ba26436d-7009-476f-23b0-45676a0e7805", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["200034"], "spl_set_id": ["9a57a63e-f856-aafa-037a-c08f2fea6496"], "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 (55111-163-01)", "package_ndc": "55111-163-01", "marketing_start_date": "20120423"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (55111-163-05)", "package_ndc": "55111-163-05", "marketing_start_date": "20120423"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (55111-163-30)", "package_ndc": "55111-163-30", "marketing_start_date": "20120423"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-163-78)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-163-79)", "package_ndc": "55111-163-78", "marketing_start_date": "20120423"}], "brand_name": "Olanzapine", "product_id": "55111-163_ba26436d-7009-476f-23b0-45676a0e7805", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "55111-163", "generic_name": "Olanzapine", "labeler_name": "Dr. Reddy's Laboratories Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "2.5 mg/1"}], "application_number": "ANDA076255", "marketing_category": "ANDA", "marketing_start_date": "20120423", "listing_expiration_date": "20261231"}