Package 72162-1502-1

Brand: dexmethylphenidate hydrochloride extended-release

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1502-1
Digits Only 7216215021
Product NDC 72162-1502
Product ID 72162-1502_51f04bf3-77fc-4f1a-a024-ef3d7ede8955
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1502-1)

Marketing

Marketing Status
Marketed Since 2013-11-19
Brand dexmethylphenidate hydrochloride extended-release
Generic dexmethylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Dexmethylphenidate Hydrochloride Extended-Release ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "51f04bf3-77fc-4f1a-a024-ef3d7ede8955", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899461"], "spl_set_id": ["32b3c189-f0f8-4f3e-87da-ce56f583fc42"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1502-1)", "package_ndc": "72162-1502-1", "marketing_start_date": "20131119"}], "brand_name": "Dexmethylphenidate Hydrochloride Extended-Release", "product_id": "72162-1502_51f04bf3-77fc-4f1a-a024-ef3d7ede8955", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-1502", "dea_schedule": "CII", "generic_name": "Dexmethylphenidate Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate Hydrochloride", "brand_name_suffix": "Extended-Release", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA078992", "marketing_category": "ANDA", "marketing_start_date": "20131119", "listing_expiration_date": "20261231"}