Package 72162-2429-1

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2429-1
Digits Only 7216224291
Product NDC 72162-2429
Product ID 72162-2429_350721f3-07c6-4b0f-b345-2058f4ff1f49
Description

100 TABLET in 1 BOTTLE (72162-2429-1)

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": "350721f3-07c6-4b0f-b345-2058f4ff1f49", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091150"], "spl_set_id": ["b77128b3-fce4-4bee-bdad-5fe4af9d612d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2429-1)", "package_ndc": "72162-2429-1", "marketing_start_date": "20241118"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "72162-2429_350721f3-07c6-4b0f-b345-2058f4ff1f49", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-2429", "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": "10 mg/1"}], "application_number": "ANDA208737", "marketing_category": "ANDA", "marketing_start_date": "20240416", "listing_expiration_date": "20261231"}