Package 0406-8959-01

Brand: dextroamphetamine sulfate

Generic: dextroamphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 0406-8959-01
Digits Only 0406895901
Product NDC 0406-8959
Description

100 TABLET in 1 BOTTLE (0406-8959-01)

Marketing

Marketing Status
Marketed Since 2002-01-29
Brand dextroamphetamine sulfate
Generic dextroamphetamine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f843d278-cec1-438f-8d54-120524010ce9", "openfda": {"upc": ["0304068958014", "0304068959011"], "unii": ["JJ768O327N"], "rxcui": ["884385", "884386"], "spl_set_id": ["e05cf690-d45a-4696-a1bf-40c9350cc084"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0406-8959-01)", "package_ndc": "0406-8959-01", "marketing_start_date": "20020129"}], "brand_name": "DEXTROAMPHETAMINE SULFATE", "product_id": "0406-8959_f843d278-cec1-438f-8d54-120524010ce9", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0406-8959", "dea_schedule": "CII", "generic_name": "dextroamphetamine sulfate", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXTROAMPHETAMINE SULFATE", "active_ingredients": [{"name": "DEXTROAMPHETAMINE SULFATE", "strength": "10 mg/1"}], "application_number": "ANDA040436", "marketing_category": "ANDA", "marketing_start_date": "20020129", "listing_expiration_date": "20261231"}