Package 72162-1286-1

Brand: dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1286-1
Digits Only 7216212861
Product NDC 72162-1286
Product ID 72162-1286_5dea27aa-7140-44c3-a81f-8edce5854412
Description

100 TABLET in 1 BOTTLE, PLASTIC (72162-1286-1)

Marketing

Marketing Status
Marketed Since 2024-02-01
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": "5dea27aa-7140-44c3-a81f-8edce5854412", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899548"], "spl_set_id": ["f65759db-5294-4e82-bb3c-3ea368edaca7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72162-1286-1)", "package_ndc": "72162-1286-1", "marketing_start_date": "20240201"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "72162-1286_5dea27aa-7140-44c3-a81f-8edce5854412", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-1286", "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": "ANDA207901", "marketing_category": "ANDA", "marketing_start_date": "20011130", "listing_expiration_date": "20261231"}