Package 27808-090-01

Brand: dextroamphetamine sulfate

Generic: dextroamphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 27808-090-01
Digits Only 2780809001
Product NDC 27808-090
Description

100 TABLET in 1 BOTTLE, PLASTIC (27808-090-01)

Marketing

Marketing Status
Marketed Since 2023-02-28
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": "97577638-7333-40a8-87d8-f426b7ee7672", "openfda": {"unii": ["JJ768O327N"], "rxcui": ["884385", "884386"], "spl_set_id": ["9acdf000-fefe-47c7-a44c-0f7a65c5c05c"], "manufacturer_name": ["Cranbury Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (27808-090-01)", "package_ndc": "27808-090-01", "marketing_start_date": "20230228"}], "brand_name": "Dextroamphetamine Sulfate", "product_id": "27808-090_97577638-7333-40a8-87d8-f426b7ee7672", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "27808-090", "dea_schedule": "CII", "generic_name": "Dextroamphetamine Sulfate", "labeler_name": "Cranbury Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextroamphetamine Sulfate", "active_ingredients": [{"name": "DEXTROAMPHETAMINE SULFATE", "strength": "10 mg/1"}], "application_number": "ANDA206095", "marketing_category": "ANDA", "marketing_start_date": "20220820", "listing_expiration_date": "20261231"}