Package 0406-1445-01

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0406-1445-01
Digits Only 0406144501
Product NDC 0406-1445
Product ID 0406-1445_7bfd27d5-70ed-440b-949a-140aa3304d4a
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0406-1445-01)

Marketing

Marketing Status
Marketed Since 2000-05-09
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": "7bfd27d5-70ed-440b-949a-140aa3304d4a", "openfda": {"upc": ["0304061473019", "0304061445016"], "unii": ["4B3SC438HI"], "rxcui": ["1091145", "1091225"], "spl_set_id": ["ed004cf0-eb23-43d2-96dc-20c4ad63824f"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0406-1445-01)", "package_ndc": "0406-1445-01", "marketing_start_date": "20000509"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "0406-1445_7bfd27d5-70ed-440b-949a-140aa3304d4a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0406-1445", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA075629", "marketing_category": "ANDA", "marketing_start_date": "20000509", "listing_expiration_date": "20261231"}