Package 0078-0440-05

Brand: ritalin

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0078-0440-05
Digits Only 0078044005
Product NDC 0078-0440
Description

100 TABLET in 1 BOTTLE (0078-0440-05)

Marketing

Marketing Status
Discontinued 2026-07-31
Brand ritalin
Generic methylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "00db4d6e-410b-43a1-ab5e-7047f525e68d", "openfda": {"upc": ["0300780441056", "0300780439053"], "unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091379", "1091392", "1091395", "1091497", "1091500"], "spl_set_id": ["c0bf0835-6a2f-4067-a158-8b86c4b0668a"], "manufacturer_name": ["Novartis Pharmaceuticals Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0078-0440-05)", "package_ndc": "0078-0440-05", "marketing_end_date": "20260731", "marketing_start_date": "19551231"}], "brand_name": "Ritalin", "product_id": "0078-0440_00db4d6e-410b-43a1-ab5e-7047f525e68d", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0078-0440", "dea_schedule": "CII", "generic_name": "methylphenidate hydrochloride", "labeler_name": "Novartis Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ritalin", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA010187", "marketing_category": "NDA", "marketing_end_date": "20260831", "marketing_start_date": "19551231"}