Package 0115-1686-01

Brand: dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0115-1686-01
Digits Only 0115168601
Product NDC 0115-1686
Product ID 0115-1686_d431fe33-4a29-4d90-9d0d-38f146aedbd6
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0115-1686-01)

Marketing

Marketing Status
Marketed Since 2014-02-24
Brand dexmethylphenidate hydrochloride
Generic dexmethylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Dexmethylphenidate hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d431fe33-4a29-4d90-9d0d-38f146aedbd6", "openfda": {"upc": ["0301151683013", "0301151686014", "0301151682016", "0301151684010", "0301151685017"], "unii": ["1678OK0E08"], "rxcui": ["899439", "899461", "899485", "899495", "899511"], "spl_set_id": ["5312f2c3-bd73-4d29-b8d1-e989282be750"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0115-1686-01)", "package_ndc": "0115-1686-01", "marketing_start_date": "20140224"}], "brand_name": "Dexmethylphenidate hydrochloride", "product_id": "0115-1686_d431fe33-4a29-4d90-9d0d-38f146aedbd6", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0115-1686", "dea_schedule": "CII", "generic_name": "Dexmethylphenidate hydrochloride", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate hydrochloride", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA079108", "marketing_category": "ANDA", "marketing_start_date": "20140224", "listing_expiration_date": "20261231"}