Package 72162-2019-6

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2019-6
Digits Only 7216220196
Product NDC 72162-2019
Description

60 TABLET in 1 BOTTLE (72162-2019-6)

Marketing

Marketing Status
Marketed Since 2024-04-03
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": "13a17c5a-bba7-4c5a-a4f9-2141bcdffa1a", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091497"], "spl_set_id": ["13a17c5a-bba7-4c5a-a4f9-2141bcdffa1a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2019-1)", "package_ndc": "72162-2019-1", "marketing_start_date": "20240403"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72162-2019-6)", "package_ndc": "72162-2019-6", "marketing_start_date": "20240403"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "72162-2019_13a17c5a-bba7-4c5a-a4f9-2141bcdffa1a", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-2019", "dea_schedule": "CII", "generic_name": "METHYLPHENIDATE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "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"}