Package 43547-458-10
Brand: amphetamine sulfate
Generic: amphetamine sulfatePackage Facts
Identity
Package NDC
43547-458-10
Digits Only
4354745810
Product NDC
43547-458
Description
100 TABLET in 1 BOTTLE (43547-458-10)
Marketing
Marketing Status
Brand
amphetamine sulfate
Generic
amphetamine sulfate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b11d796e-584c-49a4-9f05-b499f5cd0f5e", "openfda": {"unii": ["6DPV8NK46S"], "rxcui": ["884655", "1600695"], "spl_set_id": ["89c5b52f-3c2a-41d5-8624-9ee51c512c72"], "manufacturer_name": ["Solco Healthcare US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (43547-458-10)", "package_ndc": "43547-458-10", "marketing_start_date": "20200402"}], "brand_name": "AMPHETAMINE SULFATE", "product_id": "43547-458_b11d796e-584c-49a4-9f05-b499f5cd0f5e", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "43547-458", "dea_schedule": "CII", "generic_name": "amphetamine sulfate", "labeler_name": "Solco Healthcare US, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMPHETAMINE SULFATE", "active_ingredients": [{"name": "AMPHETAMINE SULFATE", "strength": "10 mg/1"}], "application_number": "ANDA211861", "marketing_category": "ANDA", "marketing_start_date": "20200402", "listing_expiration_date": "20261231"}