Package 0527-4580-37

Brand: methylphenidate hydrochloride cd

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0527-4580-37
Digits Only 0527458037
Product NDC 0527-4580
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4580-37)

Marketing

Marketing Status
Marketed Since 2003-02-18
Brand methylphenidate hydrochloride cd
Generic methylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bd13224e-942e-4866-88b9-8729c89204e7", "openfda": {"upc": ["0305274579376", "0305274580372", "0305274584370"], "unii": ["4B3SC438HI"], "rxcui": ["1806181", "1806187", "1806189", "1806191", "1806193", "1806197"], "spl_set_id": ["e45c75dc-d381-475b-b649-a871c8a36e60"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4580-37)", "package_ndc": "0527-4580-37", "marketing_start_date": "20030218"}], "brand_name": "methylphenidate hydrochloride CD", "product_id": "0527-4580_bd13224e-942e-4866-88b9-8729c89204e7", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0527-4580", "dea_schedule": "CII", "generic_name": "methylphenidate hydrochloride", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "methylphenidate hydrochloride CD", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "NDA021259", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20030218", "listing_expiration_date": "20261231"}