Package 72162-2427-1

Brand: dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2427-1
Digits Only 7216224271
Product NDC 72162-2427
Product ID 72162-2427_e14f6aaf-eaec-45cb-8fba-839a3f4609d3
Description

100 TABLET in 1 BOTTLE (72162-2427-1)

Marketing

Marketing Status
Marketed Since 2024-11-18
Brand dexmethylphenidate hydrochloride
Generic dexmethylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Dexmethylphenidate hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e14f6aaf-eaec-45cb-8fba-839a3f4609d3", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899548"], "spl_set_id": ["76aa2130-2b7b-40f7-a35a-d51b21da4636"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2427-1)", "package_ndc": "72162-2427-1", "marketing_start_date": "20241118"}], "brand_name": "Dexmethylphenidate hydrochloride", "product_id": "72162-2427_e14f6aaf-eaec-45cb-8fba-839a3f4609d3", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-2427", "dea_schedule": "CII", "generic_name": "Dexmethylphenidate hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate hydrochloride", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209211", "marketing_category": "ANDA", "marketing_start_date": "20240503", "listing_expiration_date": "20261231"}