Package 70518-1613-0

Brand: risperidone

Generic: risperidone
NDC Package

Package Facts

Identity

Package NDC 70518-1613-0
Digits Only 7051816130
Product NDC 70518-1613
Description

30 TABLET in 1 BLISTER PACK (70518-1613-0)

Marketing

Marketing Status
Marketed Since 2018-10-29
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": "494f91d6-a715-bccd-e063-6294a90a0b7f", "openfda": {"nui": ["N0000175430"], "unii": ["L6UH7ZF8HC"], "rxcui": ["314211"], "spl_set_id": ["101b2d4d-4740-4225-94bc-aecc05d82c6b"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1613-0)", "package_ndc": "70518-1613-0", "marketing_start_date": "20181029"}], "brand_name": "RISPERIDONE", "product_id": "70518-1613_494f91d6-a715-bccd-e063-6294a90a0b7f", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-1613", "generic_name": "RISPERIDONE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RISPERIDONE", "active_ingredients": [{"name": "RISPERIDONE", "strength": "4 mg/1"}], "application_number": "ANDA201003", "marketing_category": "ANDA", "marketing_start_date": "20181029", "listing_expiration_date": "20271231"}