Package 69238-1563-1

Brand: amphetamine sulfate

Generic: amphetamine
NDC Package

Package Facts

Identity

Package NDC 69238-1563-1
Digits Only 6923815631
Product NDC 69238-1563
Product ID 69238-1563_940571ac-35e3-426e-8eb0-386a3987c3b9
Description

100 TABLET in 1 BOTTLE (69238-1563-1)

Marketing

Marketing Status
Marketed Since 2018-09-28
Brand amphetamine sulfate
Generic amphetamine
Sample Package No

Linked Drug Pages (1)

Amphetamine Sulfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "940571ac-35e3-426e-8eb0-386a3987c3b9", "openfda": {"unii": ["6DPV8NK46S"], "rxcui": ["884655", "1600695"], "spl_set_id": ["53d40847-e0d3-48ec-81a7-ec5478553565"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69238-1563-1)", "package_ndc": "69238-1563-1", "marketing_start_date": "20180928"}], "brand_name": "Amphetamine Sulfate", "product_id": "69238-1563_940571ac-35e3-426e-8eb0-386a3987c3b9", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "69238-1563", "dea_schedule": "CII", "generic_name": "Amphetamine", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amphetamine Sulfate", "active_ingredients": [{"name": "AMPHETAMINE SULFATE", "strength": "5 mg/1"}], "application_number": "ANDA211139", "marketing_category": "ANDA", "marketing_start_date": "20180928", "listing_expiration_date": "20261231"}