Package 63629-1172-1

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1172-1
Digits Only 6362911721
Product NDC 63629-1172
Product ID 63629-1172_f369071e-c6e4-4f7d-925d-4c09eb466f75
Description

100 TABLET in 1 BOTTLE (63629-1172-1)

Marketing

Marketing Status
Marketed Since 2013-08-16
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": "f369071e-c6e4-4f7d-925d-4c09eb466f75", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091497"], "spl_set_id": ["1c7d7e6c-4e96-4d18-8dca-203ef50766ec"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-1172-1)", "package_ndc": "63629-1172-1", "marketing_start_date": "20130816"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "63629-1172_f369071e-c6e4-4f7d-925d-4c09eb466f75", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "63629-1172", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090710", "marketing_category": "ANDA", "marketing_start_date": "20130816", "listing_expiration_date": "20261231"}