Package 63629-2305-1

Brand: dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2305-1
Digits Only 6362923051
Product NDC 63629-2305
Product ID 63629-2305_a94ee633-3b2f-4f07-b250-f061c7d890e4
Description

100 TABLET in 1 BOTTLE, PLASTIC (63629-2305-1)

Marketing

Marketing Status
Marketed Since 2021-12-22
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": "a94ee633-3b2f-4f07-b250-f061c7d890e4", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899557"], "spl_set_id": ["194bb3a5-5f6c-49e3-85ab-ac557b3f8bbd"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (63629-2305-1)", "package_ndc": "63629-2305-1", "marketing_start_date": "20211222"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "63629-2305_a94ee633-3b2f-4f07-b250-f061c7d890e4", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "63629-2305", "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": "2.5 mg/1"}], "application_number": "ANDA207901", "marketing_category": "ANDA", "marketing_start_date": "20011130", "listing_expiration_date": "20261231"}