Package 65862-658-03
Brand: olanzapine
Generic: olanzapinePackage Facts
Identity
Package NDC
65862-658-03
Digits Only
6586265803
Product NDC
65862-658
Description
3 BLISTER PACK in 1 CARTON (65862-658-03) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (65862-658-10)
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": "4f9fe058-fa71-4b85-9bad-482ade6b085e", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312076", "314155", "351107", "351108"], "spl_set_id": ["4d768cfe-3b20-4127-95b9-b4151b28afcc"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (65862-658-03) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (65862-658-10)", "package_ndc": "65862-658-03", "marketing_start_date": "20140515"}], "brand_name": "Olanzapine", "product_id": "65862-658_4f9fe058-fa71-4b85-9bad-482ade6b085e", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "65862-658", "generic_name": "Olanzapine", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "15 mg/1"}], "application_number": "ANDA203708", "marketing_category": "ANDA", "marketing_start_date": "20140515", "listing_expiration_date": "20271231"}