Package 66758-252-01

Brand: focalin

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 66758-252-01
Digits Only 6675825201
Product NDC 66758-252
Product ID 66758-252_b5989bf2-41d3-4bd9-82aa-d89923911cd1
Description

100 TABLET in 1 BOTTLE (66758-252-01)

Marketing

Marketing Status
Discontinued 2027-04-30
Brand focalin
Generic dexmethylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Focalin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b5989bf2-41d3-4bd9-82aa-d89923911cd1", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899518", "899519", "899548", "899549", "899557", "899559"], "spl_set_id": ["2016f5c2-95d2-4655-af65-c588c2bf5e6d"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (66758-252-01)", "package_ndc": "66758-252-01", "marketing_end_date": "20270430", "marketing_start_date": "20240712"}], "brand_name": "Focalin", "product_id": "66758-252_b5989bf2-41d3-4bd9-82aa-d89923911cd1", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "66758-252", "dea_schedule": "CII", "generic_name": "dexmethylphenidate hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Focalin", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA021278", "marketing_category": "NDA", "marketing_end_date": "20270930", "marketing_start_date": "20011130"}