Package 72162-2353-3

Brand: dextroamphetamine sulfate

Generic: dextroamphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 72162-2353-3
Digits Only 7216223533
Product NDC 72162-2353
Product ID 72162-2353_ce15c3db-cae3-4697-9bcc-20d3ba949d4d
Description

30 TABLET in 1 BOTTLE (72162-2353-3)

Marketing

Marketing Status
Marketed Since 2024-08-14
Brand dextroamphetamine sulfate
Generic dextroamphetamine sulfate
Sample Package No

Linked Drug Pages (1)

Dextroamphetamine Sulfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ce15c3db-cae3-4697-9bcc-20d3ba949d4d", "openfda": {"unii": ["JJ768O327N"], "rxcui": ["1535470"], "spl_set_id": ["9f1c9cb0-7752-40cc-8ed1-5e79b8dc9da2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2353-3)", "package_ndc": "72162-2353-3", "marketing_start_date": "20240814"}], "brand_name": "Dextroamphetamine Sulfate", "product_id": "72162-2353_ce15c3db-cae3-4697-9bcc-20d3ba949d4d", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-2353", "dea_schedule": "CII", "generic_name": "Dextroamphetamine Sulfate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextroamphetamine Sulfate", "active_ingredients": [{"name": "DEXTROAMPHETAMINE SULFATE", "strength": "30 mg/1"}], "application_number": "ANDA090533", "marketing_category": "ANDA", "marketing_start_date": "20210806", "listing_expiration_date": "20261231"}