Package 0591-3851-01

Brand: vigabatrin

Generic: vigabatrin
NDC Package

Package Facts

Identity

Package NDC 0591-3851-01
Digits Only 0591385101
Product NDC 0591-3851
Product ID 0591-3851_c29a7450-ee68-466a-a33f-bf5065da1593
Description

100 TABLET, FILM COATED in 1 BOTTLE (0591-3851-01)

Marketing

Marketing Status
Marketed Since 2019-02-06
Brand vigabatrin
Generic vigabatrin
Sample Package No

Linked Drug Pages (1)

Vigabatrin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c29a7450-ee68-466a-a33f-bf5065da1593", "openfda": {"nui": ["N0000175753"], "unii": ["GR120KRT6K"], "rxcui": ["199521"], "spl_set_id": ["8dc7bd15-2636-4d58-b651-dd117ca43dbd"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0591-3851-01)", "package_ndc": "0591-3851-01", "marketing_start_date": "20190206"}], "brand_name": "Vigabatrin", "product_id": "0591-3851_c29a7450-ee68-466a-a33f-bf5065da1593", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]"], "product_ndc": "0591-3851", "generic_name": "Vigabatrin", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vigabatrin", "active_ingredients": [{"name": "VIGABATRIN", "strength": "500 mg/1"}], "application_number": "ANDA209822", "marketing_category": "ANDA", "marketing_start_date": "20190206", "listing_expiration_date": "20261231"}