Package 57664-379-18

Brand: dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 57664-379-18
Digits Only 5766437918
Product NDC 57664-379
Product ID 57664-379_0d0cbfc3-ae27-b481-e063-6394a90a917c
Description

1000 TABLET in 1 BOTTLE (57664-379-18)

Marketing

Marketing Status
Marketed Since 2013-09-26
Brand dexmethylphenidate hydrochloride
Generic dexmethylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Dexmethylphenidate hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0d0cbfc3-ae27-b481-e063-6394a90a917c", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899518", "899548", "899557"], "spl_set_id": ["987b4983-1edc-40f1-adc9-724747080969"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (57664-379-08)", "package_ndc": "57664-379-08", "marketing_start_date": "20130926"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (57664-379-13)", "package_ndc": "57664-379-13", "marketing_start_date": "20130926"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (57664-379-18)", "package_ndc": "57664-379-18", "marketing_start_date": "20130926"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (57664-379-83)", "package_ndc": "57664-379-83", "marketing_start_date": "20130926"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (57664-379-88)", "package_ndc": "57664-379-88", "marketing_start_date": "20130926"}], "brand_name": "Dexmethylphenidate hydrochloride", "product_id": "57664-379_0d0cbfc3-ae27-b481-e063-6394a90a917c", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "57664-379", "dea_schedule": "CII", "generic_name": "Dexmethylphenidate hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate hydrochloride", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA201231", "marketing_category": "ANDA", "marketing_start_date": "20130926", "listing_expiration_date": "20261231"}