Package 72162-2041-5

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2041-5
Digits Only 7216220415
Product NDC 72162-2041
Product ID 72162-2041_d20ea2d7-adf3-4d51-874b-8e778b55991c
Description

500 mL in 1 BOTTLE, PLASTIC (72162-2041-5)

Marketing

Marketing Status
Marketed Since 2024-04-03
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": "d20ea2d7-adf3-4d51-874b-8e778b55991c", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091133"], "spl_set_id": ["83e70f8f-18dd-45fc-8bc5-4b8f7f23439e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE, PLASTIC (72162-2041-5)", "package_ndc": "72162-2041-5", "marketing_start_date": "20240403"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "72162-2041_d20ea2d7-adf3-4d51-874b-8e778b55991c", "dosage_form": "SOLUTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-2041", "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/5mL"}], "application_number": "ANDA091601", "marketing_category": "ANDA", "marketing_start_date": "20150304", "listing_expiration_date": "20261231"}