Package 0115-1710-01

Brand: dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0115-1710-01
Digits Only 0115171001
Product NDC 0115-1710
Product ID 0115-1710_b9254c68-2d68-4a6d-874b-d85a32ce4893
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0115-1710-01)

Marketing

Marketing Status
Marketed Since 2017-07-05
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": "b9254c68-2d68-4a6d-874b-d85a32ce4893", "openfda": {"upc": ["0301151710016", "0301151709010"], "unii": ["1678OK0E08"], "rxcui": ["1101926", "1101932"], "spl_set_id": ["be7019d7-eb3e-48eb-b6ba-0ffefae6dcd0"], "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 (0115-1710-01)", "package_ndc": "0115-1710-01", "marketing_start_date": "20170705"}], "brand_name": "Dexmethylphenidate hydrochloride", "product_id": "0115-1710_b9254c68-2d68-4a6d-874b-d85a32ce4893", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0115-1710", "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": "35 mg/1"}], "application_number": "ANDA203614", "marketing_category": "ANDA", "marketing_start_date": "20170705", "listing_expiration_date": "20261231"}