Package 72516-015-01
Brand: dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfate
Generic: dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfatePackage Facts
Identity
Package NDC
72516-015-01
Digits Only
7251601501
Product NDC
72516-015
Description
100 TABLET in 1 BOTTLE (72516-015-01)
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": "39fb17a2-617d-37dc-e063-6394a90a1be3", "openfda": {"unii": ["O1ZPV620O4", "6DPV8NK46S", "G83415V073", "JJ768O327N"], "rxcui": ["541363", "541878", "541892", "577957", "577961", "1009145"], "spl_set_id": ["acd27181-a3f3-4c38-85d8-029a4a82e7c2"], "manufacturer_name": ["Oryza Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72516-015-01)", "package_ndc": "72516-015-01", "marketing_start_date": "20201019"}], "brand_name": "Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate", "product_id": "72516-015_39fb17a2-617d-37dc-e063-6394a90a1be3", "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": "72516-015", "dea_schedule": "CII", "generic_name": "Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate", "labeler_name": "Oryza Pharmaceuticals Inc.", "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": "ANDA210293", "marketing_category": "ANDA", "marketing_start_date": "20201019", "listing_expiration_date": "20261231"}