Package 72162-2043-2

Brand: dextroamphetamine

Generic: dextroamphetamine
NDC Package

Package Facts

Identity

Package NDC 72162-2043-2
Digits Only 7216220432
Product NDC 72162-2043
Product ID 72162-2043_9dcba5a8-b4ee-4e3c-a0be-3587072a4c5a
Description

473 mL in 1 BOTTLE, PLASTIC (72162-2043-2)

Marketing

Marketing Status
Marketed Since 2024-04-03
Brand dextroamphetamine
Generic dextroamphetamine
Sample Package No

Linked Drug Pages (1)

Dextroamphetamine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9dcba5a8-b4ee-4e3c-a0be-3587072a4c5a", "openfda": {"unii": ["JJ768O327N"], "rxcui": ["884522"], "spl_set_id": ["76da9845-2ce1-49a5-9bf3-6a550d623172"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (72162-2043-2)", "package_ndc": "72162-2043-2", "marketing_start_date": "20240403"}], "brand_name": "Dextroamphetamine", "product_id": "72162-2043_9dcba5a8-b4ee-4e3c-a0be-3587072a4c5a", "dosage_form": "SOLUTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-2043", "dea_schedule": "CII", "generic_name": "Dextroamphetamine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextroamphetamine", "active_ingredients": [{"name": "DEXTROAMPHETAMINE SULFATE", "strength": "5 mg/5mL"}], "application_number": "ANDA203644", "marketing_category": "ANDA", "marketing_start_date": "20130531", "listing_expiration_date": "20261231"}