Package 0093-5550-01

Brand: dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-5550-01
Digits Only 0093555001
Product NDC 0093-5550
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5550-01)

Marketing

Marketing Status
Marketed Since 2014-11-10
Brand dexmethylphenidate hydrochloride
Generic dexmethylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ee2dd90b-be3b-4649-b6f8-91468a37b1a5", "openfda": {"upc": ["0300935046013"], "unii": ["1678OK0E08"], "rxcui": ["899439", "899461", "899485", "899495", "899511", "1006608", "1101926", "1101932"], "spl_set_id": ["dd659d39-41f5-4612-8f17-bad602b4784d"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5550-01)", "package_ndc": "0093-5550-01", "marketing_start_date": "20141110"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "0093-5550_ee2dd90b-be3b-4649-b6f8-91468a37b1a5", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0093-5550", "dea_schedule": "CII", "generic_name": "Dexmethylphenidate Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate Hydrochloride", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA078908", "marketing_category": "ANDA", "marketing_start_date": "20141110", "listing_expiration_date": "20261231"}