Package 0781-2364-01

Brand: methylphenidate

Generic: methylphenidate
NDC Package

Package Facts

Identity

Package NDC 0781-2364-01
Digits Only 0781236401
Product NDC 0781-2364
Product ID 0781-2364_2a42277a-d670-4bae-b49d-fd1d8e13afff
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2364-01)

Marketing

Marketing Status
Discontinued 2026-10-31
Brand methylphenidate
Generic methylphenidate
Sample Package No

Linked Drug Pages (1)

Methylphenidate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a42277a-d670-4bae-b49d-fd1d8e13afff", "openfda": {"upc": ["0307812364017", "0307812362013"], "unii": ["4B3SC438HI"], "rxcui": ["1806177", "1806179", "1806183", "1806195"], "spl_set_id": ["1f8983ce-71b8-4c62-830d-e4692ddededa"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2364-01)", "package_ndc": "0781-2364-01", "marketing_end_date": "20261031", "marketing_start_date": "20151124"}], "brand_name": "Methylphenidate", "product_id": "0781-2364_2a42277a-d670-4bae-b49d-fd1d8e13afff", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0781-2364", "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": "40 mg/1"}], "application_number": "NDA021284", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20270430", "marketing_start_date": "20151124"}