Package 0378-0636-91

Brand: iloperidone

Generic: iloperidone
NDC Package

Package Facts

Identity

Package NDC 0378-0636-91
Digits Only 0378063691
Product NDC 0378-0636
Description

60 TABLET in 1 BOTTLE (0378-0636-91)

Marketing

Marketing Status
Marketed Since 2017-03-20
Brand iloperidone
Generic iloperidone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "30392c6b-2f42-6e82-e063-6394a90a0c88", "openfda": {"nui": ["N0000175430"], "upc": ["0303780631915", "0303780633919", "0303780636910", "0303780634916", "0303780632912", "0303780635913", "0303780630918"], "unii": ["VPO7KJ050N"], "rxcui": ["848722", "848728", "848732", "848736", "848740", "848744", "848748"], "spl_set_id": ["eeb0fcfd-e4e8-4fb1-9635-901dc9446235"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0378-0636-01)", "package_ndc": "0378-0636-01", "marketing_start_date": "20170320"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (0378-0636-88)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "0378-0636-88", "marketing_start_date": "20170320"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (0378-0636-91)", "package_ndc": "0378-0636-91", "marketing_start_date": "20170320"}], "brand_name": "ILOPERIDONE", "product_id": "0378-0636_30392c6b-2f42-6e82-e063-6394a90a0c88", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0378-0636", "generic_name": "iloperidone", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ILOPERIDONE", "active_ingredients": [{"name": "ILOPERIDONE", "strength": "12 mg/1"}], "application_number": "ANDA207231", "marketing_category": "ANDA", "marketing_start_date": "20170320", "listing_expiration_date": "20261231"}