Package 68382-112-10

Brand: risperidone

Generic: risperidone
NDC Package

Package Facts

Identity

Package NDC 68382-112-10
Digits Only 6838211210
Product NDC 68382-112
Description

1000 TABLET, FILM COATED in 1 BOTTLE (68382-112-10)

Marketing

Marketing Status
Marketed Since 2008-11-13
Brand risperidone
Generic risperidone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2af53e64-46a6-4b12-9ac8-8f8031a8bd97", "openfda": {"nui": ["N0000175430"], "unii": ["L6UH7ZF8HC"], "rxcui": ["312828", "312829", "312830", "312831", "312832", "314211"], "spl_set_id": ["713b5ac7-53d6-4139-8599-3028f789de4b"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68382-112-01)", "package_ndc": "68382-112-01", "marketing_start_date": "20081113"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (68382-112-05)", "package_ndc": "68382-112-05", "marketing_start_date": "20081113"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68382-112-06)", "package_ndc": "68382-112-06", "marketing_start_date": "20081113"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (68382-112-10)", "package_ndc": "68382-112-10", "marketing_start_date": "20081113"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68382-112-14)", "package_ndc": "68382-112-14", "marketing_start_date": "20081113"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68382-112-16)", "package_ndc": "68382-112-16", "marketing_start_date": "20081113"}], "brand_name": "risperidone", "product_id": "68382-112_2af53e64-46a6-4b12-9ac8-8f8031a8bd97", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68382-112", "generic_name": "risperidone", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "risperidone", "active_ingredients": [{"name": "RISPERIDONE", "strength": ".25 mg/1"}], "application_number": "ANDA078040", "marketing_category": "ANDA", "marketing_start_date": "20081113", "listing_expiration_date": "20261231"}