Package 63629-2173-1

Brand: dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2173-1
Digits Only 6362921731
Product NDC 63629-2173
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2173-1)

Marketing

Marketing Status
Marketed Since 2024-08-08
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": "6eafcf43-b88e-452f-8946-0136b435a90b", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899485"], "spl_set_id": ["424da264-7448-4364-939f-d3ebbee1a6d7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2173-1)", "package_ndc": "63629-2173-1", "marketing_start_date": "20240808"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "63629-2173_6eafcf43-b88e-452f-8946-0136b435a90b", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "63629-2173", "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": "20 mg/1"}], "application_number": "ANDA202842", "marketing_category": "ANDA", "marketing_start_date": "20170105", "listing_expiration_date": "20261231"}