Package 57664-230-88

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 57664-230-88
Digits Only 5766423088
Product NDC 57664-230
Product ID 57664-230_2f1c1df8-491a-08c9-e063-6394a90a1d06
Description

100 TABLET in 1 BOTTLE (57664-230-88)

Marketing

Marketing Status
Marketed Since 2013-08-16
Brand methylphenidate hydrochloride
Generic methylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Methylphenidate Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2f1c1df8-491a-08c9-e063-6394a90a1d06", "openfda": {"upc": ["0357664228883", "0357664229880", "0357664230886"], "unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091392", "1091497"], "spl_set_id": ["1a89b390-0cd5-45cb-9e70-20de44652c56"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (57664-230-08)", "package_ndc": "57664-230-08", "marketing_start_date": "20130816"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (57664-230-13)", "package_ndc": "57664-230-13", "marketing_start_date": "20130816"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (57664-230-18)", "package_ndc": "57664-230-18", "marketing_start_date": "20130816"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (57664-230-83)", "package_ndc": "57664-230-83", "marketing_start_date": "20130816"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (57664-230-88)", "package_ndc": "57664-230-88", "marketing_start_date": "20130816"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "57664-230_2f1c1df8-491a-08c9-e063-6394a90a1d06", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "57664-230", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA090710", "marketing_category": "ANDA", "marketing_start_date": "20130816", "listing_expiration_date": "20261231"}