Package 27808-085-01

Brand: dextroamphetamine

Generic: dextroamphetamine
NDC Package

Package Facts

Identity

Package NDC 27808-085-01
Digits Only 2780808501
Product NDC 27808-085
Product ID 27808-085_442f3920-82b4-41ab-b485-24954a2ebddb
Description

473 mL in 1 BOTTLE, PLASTIC (27808-085-01)

Marketing

Marketing Status
Marketed Since 2013-05-31
Brand dextroamphetamine
Generic dextroamphetamine
Sample Package No

Linked Drug Pages (1)

Dextroamphetamine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "442f3920-82b4-41ab-b485-24954a2ebddb", "openfda": {"unii": ["JJ768O327N"], "rxcui": ["884522"], "spl_set_id": ["7658071e-ee2c-4d23-94ce-1906959ec036"], "manufacturer_name": ["Cranbury Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (27808-085-01)", "package_ndc": "27808-085-01", "marketing_start_date": "20130531"}], "brand_name": "Dextroamphetamine", "product_id": "27808-085_442f3920-82b4-41ab-b485-24954a2ebddb", "dosage_form": "SOLUTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "27808-085", "dea_schedule": "CII", "generic_name": "Dextroamphetamine", "labeler_name": "Cranbury Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextroamphetamine", "active_ingredients": [{"name": "DEXTROAMPHETAMINE SULFATE", "strength": "5 mg/5mL"}], "application_number": "ANDA203644", "marketing_category": "ANDA", "marketing_start_date": "20130531", "listing_expiration_date": "20261231"}