Package 43386-871-01

Brand: dextroamphetamine sulfate

Generic: dextroamphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 43386-871-01
Digits Only 4338687101
Product NDC 43386-871
Description

100 TABLET in 1 BOTTLE (43386-871-01)

Marketing

Marketing Status
Marketed Since 2016-04-25
Brand dextroamphetamine sulfate
Generic dextroamphetamine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fe1d7b03-a5d0-4a7c-99ad-7aca6edb5d02", "openfda": {"upc": ["0343386871018", "0343386870035"], "unii": ["JJ768O327N"], "rxcui": ["884385", "884386"], "spl_set_id": ["9aea6b7c-729c-484d-b625-c3591b63b350"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (43386-871-01)", "package_ndc": "43386-871-01", "marketing_start_date": "20160425"}], "brand_name": "Dextroamphetamine Sulfate", "product_id": "43386-871_fe1d7b03-a5d0-4a7c-99ad-7aca6edb5d02", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "43386-871", "dea_schedule": "CII", "generic_name": "dextroamphetamine sulfate", "labeler_name": "Lupin Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextroamphetamine Sulfate", "active_ingredients": [{"name": "DEXTROAMPHETAMINE SULFATE", "strength": "10 mg/1"}], "application_number": "ANDA204330", "marketing_category": "ANDA", "marketing_start_date": "20160425", "listing_expiration_date": "20261231"}