Package 63629-2375-1

Brand: dextroamphetamine sulfate

Generic: dextroamphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 63629-2375-1
Digits Only 6362923751
Product NDC 63629-2375
Description

100 TABLET in 1 BOTTLE (63629-2375-1)

Marketing

Marketing Status
Marketed Since 2018-07-04
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": "8f8d027a-8618-467f-8f09-e120ee4521c9", "openfda": {"unii": ["JJ768O327N"], "rxcui": ["884386"], "spl_set_id": ["466cbae8-4f67-4a65-b670-ada6a953d550"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-2375-1)", "package_ndc": "63629-2375-1", "marketing_start_date": "20180704"}], "brand_name": "DEXTROAMPHETAMINE SULFATE", "product_id": "63629-2375_8f8d027a-8618-467f-8f09-e120ee4521c9", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "63629-2375", "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": "5 mg/1"}], "application_number": "ANDA210059", "marketing_category": "ANDA", "marketing_start_date": "20180704", "listing_expiration_date": "20261231"}