Package 0781-2385-01

Brand: methylphenidate

Generic: methylphenidate
NDC Package

Package Facts

Identity

Package NDC 0781-2385-01
Digits Only 0781238501
Product NDC 0781-2385
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2385-01)

Marketing

Marketing Status
Marketed Since 2025-06-10
Brand methylphenidate
Generic methylphenidate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ade65b90-a3e4-4df4-a066-b72f161dc306", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1806177", "1806179", "1806183", "1806195"], "spl_set_id": ["44386394-d2a3-4483-abe1-6c5c634cc501"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2385-01)", "package_ndc": "0781-2385-01", "marketing_start_date": "20250610"}], "brand_name": "Methylphenidate", "product_id": "0781-2385_ade65b90-a3e4-4df4-a066-b72f161dc306", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0781-2385", "dea_schedule": "CII", "generic_name": "methylphenidate", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "NDA021284", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20151124", "listing_expiration_date": "20261231"}