Package 57664-642-08

Brand: dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate

Generic: dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 57664-642-08
Digits Only 5766464208
Product NDC 57664-642
Product ID 57664-642_177c0583-addd-49cc-e063-6394a90aa6cc
Description

100 TABLET in 1 BOTTLE, PLASTIC (57664-642-08)

Marketing

Marketing Status
Marketed Since 2003-09-09
Brand dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate
Generic dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate
Sample Package No

Linked Drug Pages (1)

Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "177c0583-addd-49cc-e063-6394a90aa6cc", "openfda": {"upc": ["0357664647080", "0357664642085", "0357664645086", "0357664644089", "0357664643082"], "unii": ["6DPV8NK46S", "G83415V073", "JJ768O327N", "H527KAP6L5"], "rxcui": ["541363", "541878", "541892", "577957", "577961", "687043", "1009145"], "spl_set_id": ["9af67219-9b37-45d0-ac52-647cbfacd296"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (57664-642-08)", "package_ndc": "57664-642-08", "marketing_start_date": "20030909"}], "brand_name": "Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate", "product_id": "57664-642_177c0583-addd-49cc-e063-6394a90aa6cc", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Central Nervous System Stimulation [PE]", "Central Nervous System Stimulation [PE]", "Central Nervous System Stimulation [PE]"], "product_ndc": "57664-642", "dea_schedule": "CII", "generic_name": "Dextroamphetamine saccharate, Amphetamine aspartate, Dextroamphetamine sulfate, and Amphetamine sulfate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate", "active_ingredients": [{"name": "AMPHETAMINE ASPARTATE", "strength": "1.875 mg/1"}, {"name": "AMPHETAMINE SULFATE", "strength": "1.875 mg/1"}, {"name": "DEXTROAMPHETAMINE SACCHARATE", "strength": "1.875 mg/1"}, {"name": "DEXTROAMPHETAMINE SULFATE", "strength": "1.875 mg/1"}], "application_number": "ANDA040480", "marketing_category": "ANDA", "marketing_start_date": "20030909", "listing_expiration_date": "20261231"}