Package 72162-1507-1

Brand: dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1507-1
Digits Only 7216215071
Product NDC 72162-1507
Product ID 72162-1507_abfdbba4-dc07-4749-b79e-ce24c866897f
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1507-1)

Marketing

Marketing Status
Marketed Since 2024-08-12
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": "abfdbba4-dc07-4749-b79e-ce24c866897f", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["1006608"], "spl_set_id": ["9700cc3d-52e9-40e4-8595-f1c56279a2e0"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1507-1)", "package_ndc": "72162-1507-1", "marketing_start_date": "20240812"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "72162-1507_abfdbba4-dc07-4749-b79e-ce24c866897f", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-1507", "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": "40 mg/1"}], "application_number": "ANDA202842", "marketing_category": "ANDA", "marketing_start_date": "20170105", "listing_expiration_date": "20261231"}