Package 43547-488-10

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43547-488-10
Digits Only 4354748810
Product NDC 43547-488
Product ID 43547-488_393f91b9-9211-479f-b422-64cc81460623
Description

100 TABLET in 1 BOTTLE (43547-488-10)

Marketing

Marketing Status
Marketed Since 2020-07-01
Brand methylphenidate hydrochloride
Generic methylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Methylphenidate hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "393f91b9-9211-479f-b422-64cc81460623", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091392", "1091497"], "spl_set_id": ["238ff743-4f25-43a3-87ac-6559d12a9d49"], "manufacturer_name": ["Solco Healthcare US,LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (43547-488-10)", "package_ndc": "43547-488-10", "marketing_start_date": "20200701"}], "brand_name": "Methylphenidate hydrochloride", "product_id": "43547-488_393f91b9-9211-479f-b422-64cc81460623", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "43547-488", "dea_schedule": "CII", "generic_name": "Methylphenidate hydrochloride", "labeler_name": "Solco Healthcare US,LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA212697", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}