Package 63187-418-60

Brand: risperidone

Generic: risperidone
NDC Package

Package Facts

Identity

Package NDC 63187-418-60
Digits Only 6318741860
Product NDC 63187-418
Description

60 TABLET, FILM COATED in 1 BOTTLE (63187-418-60)

Marketing

Marketing Status
Marketed Since 2019-01-01
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": "71435439-971d-4db3-89d2-71b74b10f57c", "openfda": {"nui": ["N0000175430"], "unii": ["L6UH7ZF8HC"], "rxcui": ["312828"], "spl_set_id": ["b611fe52-1787-47e6-8a6b-1999a4e4f22c"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-418-60)", "package_ndc": "63187-418-60", "marketing_start_date": "20190101"}], "brand_name": "risperidone", "product_id": "63187-418_71435439-971d-4db3-89d2-71b74b10f57c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "63187-418", "generic_name": "risperidone", "labeler_name": "Proficient Rx LP", "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"}