Package 72162-1473-1
Brand: dexmethylphenidate hydrochloride
Generic: dexmethylphenidate hydrochloridePackage Facts
Identity
Package NDC
72162-1473-1
Digits Only
7216214731
Product NDC
72162-1473
Description
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1473-1)
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": "4a7ad9cd-cf63-4cd3-b6d3-42703d9f9e00", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899439"], "spl_set_id": ["b82e8d08-cc4a-40a6-85a5-07717f3cb38b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1473-1)", "package_ndc": "72162-1473-1", "marketing_start_date": "20240812"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "72162-1473_4a7ad9cd-cf63-4cd3-b6d3-42703d9f9e00", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-1473", "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"}