Package 63629-2459-1

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2459-1
Digits Only 6362924591
Product NDC 63629-2459
Product ID 63629-2459_7d542695-b239-4e7f-9842-9cb41f89ef07
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2459-1)

Marketing

Marketing Status
Marketed Since 2024-10-10
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": "7d542695-b239-4e7f-9842-9cb41f89ef07", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091155"], "spl_set_id": ["76fe667d-98f5-45ce-ba2a-2739e02b5102"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2459-1)", "package_ndc": "63629-2459-1", "marketing_start_date": "20241010"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "63629-2459_7d542695-b239-4e7f-9842-9cb41f89ef07", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "63629-2459", "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": "18 mg/1"}], "application_number": "ANDA205327", "marketing_category": "ANDA", "marketing_start_date": "20170814", "listing_expiration_date": "20261231"}