Package 67877-175-30
Brand: olanzapine
Generic: olanzapinePackage Facts
Identity
Package NDC
67877-175-30
Digits Only
6787717530
Product NDC
67877-175
Description
30 TABLET in 1 BOTTLE (67877-175-30)
Marketing
Marketing Status
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": "b4d4d6f0-2b78-4882-add2-7c6218270b7f", "openfda": {"nui": ["N0000175430"], "upc": ["0367877176321", "0367877172323", "0367877173306", "0367877177304", "0367877174013"], "unii": ["N7U69T4SZR"], "rxcui": ["200034", "283639", "312077", "312078", "312079", "314154"], "spl_set_id": ["e8626e68-088d-47ff-bf06-489a778815aa"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (67877-175-01)", "package_ndc": "67877-175-01", "marketing_start_date": "20120101"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (67877-175-10)", "package_ndc": "67877-175-10", "marketing_start_date": "20120101"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (67877-175-30)", "package_ndc": "67877-175-30", "marketing_start_date": "20120101"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE (67877-175-32)", "package_ndc": "67877-175-32", "marketing_start_date": "20120101"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (67877-175-35) / 10 TABLET in 1 BLISTER PACK (67877-175-33)", "package_ndc": "67877-175-35", "marketing_start_date": "20120101"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (67877-175-85) / 10 TABLET in 1 BLISTER PACK (67877-175-33)", "package_ndc": "67877-175-85", "marketing_start_date": "20120101"}], "brand_name": "Olanzapine", "product_id": "67877-175_b4d4d6f0-2b78-4882-add2-7c6218270b7f", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "67877-175", "generic_name": "Olanzapine", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/1"}], "application_number": "ANDA202295", "marketing_category": "ANDA", "marketing_start_date": "20120101", "listing_expiration_date": "20261231"}