Package 13107-069-50

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 13107-069-50
Digits Only 1310706950
Product NDC 13107-069
Description

50 TABLET in 1 BOTTLE (13107-069-50)

Marketing

Marketing Status
Marketed Since 2013-11-27
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"}