Package 42806-029-01

Brand: amphetamine sulfate

Generic: amphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 42806-029-01
Digits Only 4280602901
Product NDC 42806-029
Product ID 42806-029_82a8caba-ccaa-4ff8-8590-9e0b97f7d5f2
Description

100 TABLET in 1 BOTTLE (42806-029-01)

Marketing

Marketing Status
Marketed Since 2020-09-18
Brand amphetamine sulfate
Generic amphetamine sulfate
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": "82a8caba-ccaa-4ff8-8590-9e0b97f7d5f2", "openfda": {"upc": ["0342806030011", "0342806029015"], "unii": ["6DPV8NK46S"], "rxcui": ["884655", "1600695"], "spl_set_id": ["432db708-91b7-4802-88c3-ceef597b91da"], "manufacturer_name": ["Epic Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42806-029-01)", "package_ndc": "42806-029-01", "marketing_start_date": "20200918"}], "brand_name": "Amphetamine Sulfate", "product_id": "42806-029_82a8caba-ccaa-4ff8-8590-9e0b97f7d5f2", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "42806-029", "dea_schedule": "CII", "generic_name": "Amphetamine Sulfate", "labeler_name": "Epic Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amphetamine Sulfate", "active_ingredients": [{"name": "AMPHETAMINE SULFATE", "strength": "5 mg/1"}], "application_number": "ANDA213980", "marketing_category": "ANDA", "marketing_start_date": "20200918", "listing_expiration_date": "20261231"}