Package 72162-2430-1

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2430-1
Digits Only 7216224301
Product NDC 72162-2430
Product ID 72162-2430_3cf7fbf3-8b3d-404e-b987-6302f6510dda
Description

100 TABLET in 1 BOTTLE (72162-2430-1)

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": "3cf7fbf3-8b3d-404e-b987-6302f6510dda", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091392"], "spl_set_id": ["c87a2000-b75c-41df-8497-7e00a9b41ad4"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2430-1)", "package_ndc": "72162-2430-1", "marketing_start_date": "20241118"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "72162-2430_3cf7fbf3-8b3d-404e-b987-6302f6510dda", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-2430", "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": "20 mg/1"}], "application_number": "ANDA208737", "marketing_category": "ANDA", "marketing_start_date": "20240416", "listing_expiration_date": "20261231"}