Package 72162-2352-3

Brand: dextroamphetamine sulfate

Generic: dextroamphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 72162-2352-3
Digits Only 7216223523
Product NDC 72162-2352
Product ID 72162-2352_ef6e3d80-5391-42d2-b6f1-9cc8082a54e3
Description

30 TABLET in 1 BOTTLE (72162-2352-3)

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": "ef6e3d80-5391-42d2-b6f1-9cc8082a54e3", "openfda": {"unii": ["JJ768O327N"], "rxcui": ["1535454"], "spl_set_id": ["b40c9a90-7e2e-48d6-adb6-2351c0ca621d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2352-3)", "package_ndc": "72162-2352-3", "marketing_start_date": "20240814"}], "brand_name": "Dextroamphetamine Sulfate", "product_id": "72162-2352_ef6e3d80-5391-42d2-b6f1-9cc8082a54e3", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-2352", "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": "20 mg/1"}], "application_number": "ANDA090533", "marketing_category": "ANDA", "marketing_start_date": "20210806", "listing_expiration_date": "20261231"}