Package 0115-1800-01

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0115-1800-01
Digits Only 0115180001
Product NDC 0115-1800
Description

100 TABLET in 1 BOTTLE, PLASTIC (0115-1800-01)

Marketing

Marketing Status
Marketed Since 2014-04-07
Brand methylphenidate hydrochloride
Generic methylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "973233cb-8cb1-4c1d-911e-649df1287843", "openfda": {"upc": ["0301151802018", "0301151800014", "0301151801011"], "unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091392", "1091497"], "spl_set_id": ["c614cf55-b462-4f7e-b19c-6d22a47e509f"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0115-1800-01)", "package_ndc": "0115-1800-01", "marketing_start_date": "20140407"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "0115-1800_973233cb-8cb1-4c1d-911e-649df1287843", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0115-1800", "dea_schedule": "CII", "generic_name": "METHYLPHENIDATE HYDROCHLORIDE", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPHENIDATE HYDROCHLORIDE", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA091159", "marketing_category": "ANDA", "marketing_start_date": "20140407", "listing_expiration_date": "20261231"}