Package 71335-2968-1

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2968-1
Digits Only 7133529681
Product NDC 71335-2968
Product ID 71335-2968_d7ed4dad-1fcc-449b-bf11-e839c7b10a56
Description

100 TABLET in 1 BOTTLE (71335-2968-1)

Marketing

Marketing Status
Marketed Since 2025-11-11
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": "d7ed4dad-1fcc-449b-bf11-e839c7b10a56", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091150"], "spl_set_id": ["9beb136f-020b-4631-b989-c1d26a9846f7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2968-1)", "package_ndc": "71335-2968-1", "marketing_start_date": "20251111"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "71335-2968_d7ed4dad-1fcc-449b-bf11-e839c7b10a56", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "71335-2968", "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"}