Package 42858-077-45

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42858-077-45
Digits Only 4285807745
Product NDC 42858-077
Description

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42858-077-45)

Marketing

Marketing Status
Marketed Since 2020-04-01
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": "1b9cf2a8-126e-4302-881b-88a699bbdcf5", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1648183", "1806200", "1806202", "1806204", "1806206", "1806208", "1806210"], "spl_set_id": ["f7a7ffd1-bc30-4db8-8391-dddf76acd639"], "manufacturer_name": ["Rhodes Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42858-077-45)", "package_ndc": "42858-077-45", "marketing_start_date": "20200401"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "42858-077_1b9cf2a8-126e-4302-881b-88a699bbdcf5", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "42858-077", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Rhodes Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "NDA205831", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200401", "listing_expiration_date": "20261231"}