Package 52536-057-03

Brand: amphetamine sulfate

Generic: amphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 52536-057-03
Digits Only 5253605703
Product NDC 52536-057
Product ID 52536-057_87867bbf-4f82-42a0-9586-a9f530be1d2a
Description

30 TABLET in 1 BOTTLE (52536-057-03)

Marketing

Marketing Status
Marketed Since 2021-01-07
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": "87867bbf-4f82-42a0-9586-a9f530be1d2a", "openfda": {"upc": ["0352536059039", "0352536057035"], "unii": ["6DPV8NK46S"], "rxcui": ["884655", "1600695"], "spl_set_id": ["91add2e3-8359-47dc-b79f-197d36b02819"], "manufacturer_name": ["Wilshire Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (52536-057-03)", "package_ndc": "52536-057-03", "marketing_start_date": "20210107"}], "brand_name": "Amphetamine Sulfate", "product_id": "52536-057_87867bbf-4f82-42a0-9586-a9f530be1d2a", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "52536-057", "dea_schedule": "CII", "generic_name": "Amphetamine Sulfate", "labeler_name": "Wilshire Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amphetamine Sulfate", "active_ingredients": [{"name": "AMPHETAMINE SULFATE", "strength": "5 mg/1"}], "application_number": "ANDA200166", "marketing_category": "ANDA", "marketing_start_date": "20180329", "listing_expiration_date": "20271231"}