Package 57664-952-88

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

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

Package Facts

Identity

Package NDC 57664-952-88
Digits Only 5766495288
Product NDC 57664-952
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (57664-952-88)

Marketing

Marketing Status
Marketed Since 2024-02-01
Brand dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, amphetamine sulfate
Generic dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, amphetamine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "10af8563-97ec-8a5e-e063-6394a90a52f8", "openfda": {"unii": ["O1ZPV620O4", "6DPV8NK46S", "G83415V073", "JJ768O327N"], "rxcui": ["1927610", "1927617", "1927630", "1927637"], "spl_set_id": ["30e515c3-a18f-499a-87c4-be8d64cfdbc6"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (57664-952-88)", "package_ndc": "57664-952-88", "marketing_start_date": "20240201"}], "brand_name": "Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, amphetamine sulfate", "product_id": "57664-952_10af8563-97ec-8a5e-e063-6394a90a52f8", "dosage_form": "CAPSULE, EXTENDED RELEASE", "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": "57664-952", "dea_schedule": "CII", "generic_name": "Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, amphetamine sulfate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, amphetamine sulfate", "active_ingredients": [{"name": "AMPHETAMINE ASPARTATE MONOHYDRATE", "strength": "9.375 mg/1"}, {"name": "AMPHETAMINE SULFATE", "strength": "9.375 mg/1"}, {"name": "DEXTROAMPHETAMINE SACCHARATE", "strength": "9.375 mg/1"}, {"name": "DEXTROAMPHETAMINE SULFATE", "strength": "9.375 mg/1"}], "application_number": "ANDA215997", "marketing_category": "ANDA", "marketing_start_date": "20240201", "listing_expiration_date": "20261231"}