Package 13811-706-10
Brand: methylphenidate hydrochloride
Generic: methylphenidate hydrochloridePackage Facts
Identity
Package NDC
13811-706-10
Digits Only
1381170610
Product NDC
13811-706
Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-706-10)
Marketing
Marketing Status
Brand
methylphenidate hydrochloride
Generic
methylphenidate hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "da71a915-393d-4af3-9e41-3fd4a25dc652", "openfda": {"upc": ["0313811706109", "0313811708103"], "unii": ["4B3SC438HI"], "rxcui": ["1091155", "1091170", "1091185", "1091210", "1995461"], "spl_set_id": ["c45dc1de-adfa-4b3c-a7dc-cffbc8eac74f"], "manufacturer_name": ["Trigen Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-706-10)", "package_ndc": "13811-706-10", "marketing_start_date": "20170814"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "13811-706_da71a915-393d-4af3-9e41-3fd4a25dc652", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "13811-706", "dea_schedule": "CII", "generic_name": "Methylphenidate hydrochloride", "labeler_name": "Trigen Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "18 mg/1"}], "application_number": "ANDA205327", "marketing_category": "ANDA", "marketing_start_date": "20170814", "listing_expiration_date": "20271231"}