Package 50268-529-15

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-529-15
Digits Only 5026852915
Product NDC 50268-529
Description

50 BLISTER PACK in 1 BOX (50268-529-15) / 1 TABLET in 1 BLISTER PACK (50268-529-11)

Marketing

Marketing Status
Marketed Since 2020-02-13
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": "47e73f94-511d-3879-e063-6394a90ab6af", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091392"], "spl_set_id": ["9e7967c8-d323-160d-e053-2995a90a323e"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-529-15)  / 1 TABLET in 1 BLISTER PACK (50268-529-11)", "package_ndc": "50268-529-15", "marketing_start_date": "20200213"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "50268-529_47e73f94-511d-3879-e063-6394a90ab6af", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "50268-529", "dea_schedule": "CII", "generic_name": "METHYLPHENIDATE HYDROCHLORIDE", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPHENIDATE HYDROCHLORIDE", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA207416", "marketing_category": "ANDA", "marketing_start_date": "20200213", "listing_expiration_date": "20271231"}