Package 72603-399-01

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72603-399-01
Digits Only 7260339901
Product NDC 72603-399
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72603-399-01)

Marketing

Marketing Status
Marketed Since 2025-02-01
Brand methylphenidate hydrochloride
Generic methylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "24936e25-28cd-53ce-e063-6294a90ad99d", "openfda": {"upc": ["0372603399011"], "unii": ["4B3SC438HI"], "rxcui": ["1995461"], "spl_set_id": ["768bf181-d0d8-49e5-9c87-cacbb069e0b2"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72603-399-01)", "package_ndc": "72603-399-01", "marketing_start_date": "20250201"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "72603-399_24936e25-28cd-53ce-e063-6294a90ad99d", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72603-399", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "72 mg/1"}], "application_number": "ANDA217229", "marketing_category": "ANDA", "marketing_start_date": "20250201", "listing_expiration_date": "20261231"}