Package 72162-1088-1

Brand: amphetamine sulfate

Generic: amphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 72162-1088-1
Digits Only 7216210881
Product NDC 72162-1088
Product ID 72162-1088_3ad894e3-78a7-4e3b-80d1-1a925fb6d9e3
Description

100 TABLET in 1 BOTTLE (72162-1088-1)

Marketing

Marketing Status
Marketed Since 2024-04-05
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": "3ad894e3-78a7-4e3b-80d1-1a925fb6d9e3", "openfda": {"unii": ["6DPV8NK46S"], "rxcui": ["1600695"], "spl_set_id": ["3ad894e3-78a7-4e3b-80d1-1a925fb6d9e3"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1088-1)", "package_ndc": "72162-1088-1", "marketing_start_date": "20240405"}], "brand_name": "AMPHETAMINE SULFATE", "product_id": "72162-1088_3ad894e3-78a7-4e3b-80d1-1a925fb6d9e3", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-1088", "dea_schedule": "CII", "generic_name": "amphetamine sulfate", "labeler_name": "Bryant Ranch Prepack", "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"}