Package 72162-1234-1

Brand: dextroamphetamine sulfate

Generic: dextroamphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 72162-1234-1
Digits Only 7216212341
Product NDC 72162-1234
Description

100 TABLET in 1 BOTTLE (72162-1234-1)

Marketing

Marketing Status
Marketed Since 2024-09-06
Brand dextroamphetamine sulfate
Generic dextroamphetamine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b436d69f-6f1c-49b8-a8a7-6c3b77add55b", "openfda": {"unii": ["JJ768O327N"], "rxcui": ["884385"], "spl_set_id": ["c706a849-9df6-43ca-9ac6-1d9ce6b8e855"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1234-1)", "package_ndc": "72162-1234-1", "marketing_start_date": "20240906"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-1234-3)", "package_ndc": "72162-1234-3", "marketing_start_date": "20240906"}], "brand_name": "DEXTROAMPHETAMINE SULFATE", "product_id": "72162-1234_b436d69f-6f1c-49b8-a8a7-6c3b77add55b", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-1234", "dea_schedule": "CII", "generic_name": "dextroamphetamine sulfate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXTROAMPHETAMINE SULFATE", "active_ingredients": [{"name": "DEXTROAMPHETAMINE SULFATE", "strength": "10 mg/1"}], "application_number": "ANDA210059", "marketing_category": "ANDA", "marketing_start_date": "20180704", "listing_expiration_date": "20261231"}