Package 52427-806-90

Brand: gralise

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 52427-806-90
Digits Only 5242780690
Product NDC 52427-806
Product ID 52427-806_44a61305-2313-59c4-8a44-98c827461735
Description

90 TABLET, FILM COATED in 1 BOTTLE (52427-806-90)

Marketing

Marketing Status
Marketed Since 2020-10-01
Brand gralise
Generic gabapentin
Sample Package No

Linked Drug Pages (1)

Gralise ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "44a61305-2313-59c4-8a44-98c827461735", "openfda": {"nui": ["N0000008486"], "upc": ["0352427850608", "0352427803901", "0352427806902", "0352427890604", "0352427804601"], "unii": ["6CW7F3G59X"], "rxcui": ["1115012", "1115013", "1806380", "1806382", "2398511", "2398512", "2634743", "2634745", "2634747", "2634749", "2634751", "2634753"], "spl_set_id": ["466273b1-c9fc-3930-c94b-aa11394d5140"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Almatica Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (52427-806-90)", "package_ndc": "52427-806-90", "marketing_start_date": "20201001"}], "brand_name": "Gralise", "product_id": "52427-806_44a61305-2313-59c4-8a44-98c827461735", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "52427-806", "generic_name": "gabapentin", "labeler_name": "Almatica Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gralise", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "NDA022544", "marketing_category": "NDA", "marketing_start_date": "20201001", "listing_expiration_date": "20261231"}