Package 72162-2428-1

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2428-1
Digits Only 7216224281
Product NDC 72162-2428
Product ID 72162-2428_436fefb7-905b-44af-a65f-e31cf87fd52a
Description

100 TABLET in 1 BOTTLE (72162-2428-1)

Marketing

Marketing Status
Marketed Since 2024-11-18
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": "436fefb7-905b-44af-a65f-e31cf87fd52a", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091497"], "spl_set_id": ["371346d1-ac7e-491c-a010-ad29cb3d567a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2428-1)", "package_ndc": "72162-2428-1", "marketing_start_date": "20241118"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "72162-2428_436fefb7-905b-44af-a65f-e31cf87fd52a", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-2428", "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": "ANDA208737", "marketing_category": "ANDA", "marketing_start_date": "20240416", "listing_expiration_date": "20261231"}