Package 43598-166-60
Brand: olanzapine
Generic: olanzapinePackage Facts
Identity
Package NDC
43598-166-60
Digits Only
4359816660
Product NDC
43598-166
Description
60 TABLET, FILM COATED in 1 BOTTLE (43598-166-60)
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": "9f9b5830-1420-24fc-73be-4a040ccb22db", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312078", "312079", "314154"], "spl_set_id": ["d474d5a9-d338-511d-5823-567c0a1bbf4d"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (43598-166-01)", "package_ndc": "43598-166-01", "marketing_start_date": "20131210"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (43598-166-05)", "package_ndc": "43598-166-05", "marketing_start_date": "20131210"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (43598-166-10)", "package_ndc": "43598-166-10", "marketing_start_date": "20131210"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (43598-166-30)", "package_ndc": "43598-166-30", "marketing_start_date": "20131210"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (43598-166-60)", "package_ndc": "43598-166-60", "marketing_start_date": "20131210"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (43598-166-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-166-79)", "package_ndc": "43598-166-78", "marketing_start_date": "20131210"}], "brand_name": "Olanzapine", "product_id": "43598-166_9f9b5830-1420-24fc-73be-4a040ccb22db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "43598-166", "generic_name": "Olanzapine", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/1"}], "application_number": "ANDA076255", "marketing_category": "ANDA", "marketing_start_date": "20131210", "listing_expiration_date": "20261231"}