Package 0527-2525-37

Brand: amphetamine sulfate

Generic: amphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 0527-2525-37
Digits Only 0527252537
Product NDC 0527-2525
Product ID 0527-2525_23880d0f-9eea-4ef3-95aa-10fc11fcfa6c
Description

100 TABLET in 1 BOTTLE (0527-2525-37)

Marketing

Marketing Status
Marketed Since 2020-06-01
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": "23880d0f-9eea-4ef3-95aa-10fc11fcfa6c", "openfda": {"upc": ["0305272524378", "0305272525375"], "unii": ["6DPV8NK46S"], "rxcui": ["884655", "1600695"], "spl_set_id": ["85a015a7-a1a0-4b04-8bc4-7aacd0c84742"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0527-2525-37)", "package_ndc": "0527-2525-37", "marketing_start_date": "20200601"}], "brand_name": "AMPHETAMINE SULFATE", "product_id": "0527-2525_23880d0f-9eea-4ef3-95aa-10fc11fcfa6c", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0527-2525", "dea_schedule": "CII", "generic_name": "amphetamine sulfate", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMPHETAMINE SULFATE", "active_ingredients": [{"name": "AMPHETAMINE SULFATE", "strength": "10 mg/1"}], "application_number": "ANDA212901", "marketing_category": "ANDA", "marketing_start_date": "20200525", "listing_expiration_date": "20261231"}