Package 63629-2171-1
Brand: dexmethylphenidate hydrochloride
Generic: dexmethylphenidate hydrochloridePackage Facts
Identity
Package NDC
63629-2171-1
Digits Only
6362921711
Product NDC
63629-2171
Description
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2171-1)
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": "e0a41322-34d7-4e37-a588-7dde63d9a2d8", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899439"], "spl_set_id": ["c423a632-e8e0-44a7-a8a8-f66cec81aa64"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2171-1)", "package_ndc": "63629-2171-1", "marketing_start_date": "20240808"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "63629-2171_e0a41322-34d7-4e37-a588-7dde63d9a2d8", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "63629-2171", "dea_schedule": "CII", "generic_name": "Dexmethylphenidate Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate Hydrochloride", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202842", "marketing_category": "ANDA", "marketing_start_date": "20170105", "listing_expiration_date": "20261231"}