Package 64980-222-01

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 64980-222-01
Digits Only 6498022201
Product NDC 64980-222
Product ID 64980-222_85d614b0-888e-461f-bc7d-3f240ed8bd0e
Description

100 TABLET, CHEWABLE in 1 BOTTLE (64980-222-01)

Marketing

Marketing Status
Marketed Since 2018-12-18
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": "85d614b0-888e-461f-bc7d-3f240ed8bd0e", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091152", "1091322", "1091389"], "spl_set_id": ["e5cb0740-813f-4dce-8c29-d7680c66e77c"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, CHEWABLE in 1 BOTTLE (64980-222-01)", "package_ndc": "64980-222-01", "marketing_start_date": "20181218"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "64980-222_85d614b0-888e-461f-bc7d-3f240ed8bd0e", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "64980-222", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA205756", "marketing_category": "ANDA", "marketing_start_date": "20181218", "listing_expiration_date": "20261231"}