Package 16729-479-01

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16729-479-01
Digits Only 1672947901
Product NDC 16729-479
Description

100 TABLET in 1 BOTTLE (16729-479-01)

Marketing

Marketing Status
Marketed Since 2020-12-17
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": "1b2d1579-1bb4-cc17-e063-6294a90a4fa7", "openfda": {"upc": ["0316729479011", "0316729480017", "0316729478014"], "unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091392", "1091497"], "spl_set_id": ["4f3c91e6-4576-4326-bdab-7d8fb7c09bb8"], "manufacturer_name": ["Accord Healthcare, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16729-479-01)", "package_ndc": "16729-479-01", "marketing_start_date": "20201217"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "16729-479_1b2d1579-1bb4-cc17-e063-6294a90a4fa7", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "16729-479", "dea_schedule": "CII", "generic_name": "METHYLPHENIDATE HYDROCHLORIDE", "labeler_name": "Accord Healthcare, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPHENIDATE HYDROCHLORIDE", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213936", "marketing_category": "ANDA", "marketing_start_date": "20201217", "listing_expiration_date": "20261231"}