Package 0406-0136-01

Brand: methylphenidate hydrochloride extended-release

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0406-0136-01
Digits Only 0406013601
Product NDC 0406-0136
Product ID 0406-0136_7a3a8731-e545-455e-83c3-888f4923e901
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0406-0136-01)

Marketing

Marketing Status
Marketed Since 2012-12-28
Brand methylphenidate hydrochloride extended-release
Generic methylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Methylphenidate Hydrochloride Extended-Release ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7a3a8731-e545-455e-83c3-888f4923e901", "openfda": {"upc": ["0304060154018", "0304060136014", "0304060127012"], "unii": ["4B3SC438HI"], "rxcui": ["2001565", "2001566", "2001568"], "spl_set_id": ["b1b0f2ff-d9df-42ab-b471-226ecf97e075"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0406-0136-01)", "package_ndc": "0406-0136-01", "marketing_start_date": "20121228"}], "brand_name": "Methylphenidate Hydrochloride Extended-Release", "product_id": "0406-0136_7a3a8731-e545-455e-83c3-888f4923e901", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0406-0136", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "brand_name_suffix": "Extended-Release", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "36 mg/1"}], "application_number": "ANDA202608", "marketing_category": "ANDA", "marketing_start_date": "20121228", "listing_expiration_date": "20261231"}