Package 55466-103-12

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55466-103-12
Digits Only 5546610312
Product NDC 55466-103
Product ID 55466-103_2df3eacd-fa7d-ac18-e063-6294a90a70b2
Description

100 TABLET in 1 BOTTLE (55466-103-12)

Marketing

Marketing Status
Marketed Since 2024-03-29
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": "2df3eacd-fa7d-ac18-e063-6294a90a70b2", "openfda": {"upc": ["0312345678906"], "unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091392", "1091497"], "spl_set_id": ["81141f59-21ca-c8b0-e053-2a91aa0a4c56"], "manufacturer_name": ["Neolpharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (55466-103-12)", "package_ndc": "55466-103-12", "marketing_start_date": "20240329"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "55466-103_2df3eacd-fa7d-ac18-e063-6294a90a70b2", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "55466-103", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Neolpharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208737", "marketing_category": "ANDA", "marketing_start_date": "20240329", "listing_expiration_date": "20261231"}