Package 13107-069-50
Brand: dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfate
Generic: dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfatePackage Facts
Identity
Package NDC
13107-069-50
Digits Only
1310706950
Product NDC
13107-069
Description
50 TABLET in 1 BOTTLE (13107-069-50)
Marketing
Marketing Status
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)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5962d880-9f18-4a57-8c95-ca0ec1e86f44", "openfda": {"upc": ["0313107070013", "0313107068010", "0313107071010", "0313107074011", "0313107073014"], "unii": ["O1ZPV620O4", "6DPV8NK46S", "G83415V073", "JJ768O327N"], "rxcui": ["541363", "541878", "541892", "577957", "577961", "687043", "1009145"], "spl_set_id": ["a582d57f-d191-4ca5-b105-585b2d8a0e3e"], "manufacturer_name": ["Aurolife Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (13107-069-01)", "package_ndc": "13107-069-01", "marketing_start_date": "20131127"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (13107-069-05)", "package_ndc": "13107-069-05", "marketing_start_date": "20131127"}, {"sample": false, "description": "250 TABLET in 1 BOTTLE (13107-069-25)", "package_ndc": "13107-069-25", "marketing_start_date": "20131127"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (13107-069-50)", "package_ndc": "13107-069-50", "marketing_start_date": "20131127"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (13107-069-99)", "package_ndc": "13107-069-99", "marketing_start_date": "20131127"}], "brand_name": "Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate", "product_id": "13107-069_5962d880-9f18-4a57-8c95-ca0ec1e86f44", "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": "13107-069", "dea_schedule": "CII", "generic_name": "Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate", "labeler_name": "Aurolife Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate", "active_ingredients": [{"name": "AMPHETAMINE ASPARTATE MONOHYDRATE", "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": "ANDA202424", "marketing_category": "ANDA", "marketing_start_date": "20131127", "listing_expiration_date": "20261231"}