Package 70010-005-01
Brand: dexmethylphenidate hydrochloride
Generic: dexmethylphenidate hydrochloridePackage Facts
Identity
Package NDC
70010-005-01
Digits Only
7001000501
Product NDC
70010-005
Description
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-005-01)
Marketing
Marketing Status
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": "412b7fd8-c12a-36c2-e063-6394a90acae6", "openfda": {"upc": ["0370010011014", "0370010010017", "0370010009011", "0370010006010", "0370010004016", "0370010007017", "0370010008014", "0370010005013"], "unii": ["1678OK0E08"], "rxcui": ["899439", "899461", "899485", "899495", "899511", "1006608", "1101926", "1101932"], "spl_set_id": ["abe6862b-3cf3-4aad-98ea-05a5fb54ebec"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-005-01)", "package_ndc": "70010-005-01", "marketing_start_date": "20201201"}], "brand_name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "product_id": "70010-005_412b7fd8-c12a-36c2-e063-6394a90acae6", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "70010-005", "dea_schedule": "CII", "generic_name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "labeler_name": "Granules Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213813", "marketing_category": "ANDA", "marketing_start_date": "20201201", "listing_expiration_date": "20261231"}