Package 72162-1493-1

Brand: dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1493-1
Digits Only 7216214931
Product NDC 72162-1493
Product ID 72162-1493_36435a90-5e2f-496b-b2aa-fb71730dd580
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1493-1)

Marketing

Marketing Status
Marketed Since 2024-08-12
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": "36435a90-5e2f-496b-b2aa-fb71730dd580", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["1101926"], "spl_set_id": ["d9c450fa-c8c5-4ff0-a263-4a9eee6f5437"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1493-1)", "package_ndc": "72162-1493-1", "marketing_start_date": "20240812"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "72162-1493_36435a90-5e2f-496b-b2aa-fb71730dd580", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-1493", "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": "25 mg/1"}], "application_number": "ANDA202842", "marketing_category": "ANDA", "marketing_start_date": "20170105", "listing_expiration_date": "20261231"}