Package 69238-1424-1

Brand: vigabatrin

Generic: vigabatrin
NDC Package

Package Facts

Identity

Package NDC 69238-1424-1
Digits Only 6923814241
Product NDC 69238-1424
Product ID 69238-1424_96ae1401-5893-4af6-9e78-b7ec25ef42ff
Description

100 TABLET in 1 BOTTLE (69238-1424-1)

Marketing

Marketing Status
Marketed Since 2022-06-27
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": "96ae1401-5893-4af6-9e78-b7ec25ef42ff", "openfda": {"nui": ["N0000175753"], "unii": ["GR120KRT6K"], "rxcui": ["199521"], "spl_set_id": ["04fef2ec-c275-405d-91b1-99a74ee8caa2"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69238-1424-1)", "package_ndc": "69238-1424-1", "marketing_start_date": "20220627"}], "brand_name": "Vigabatrin", "product_id": "69238-1424_96ae1401-5893-4af6-9e78-b7ec25ef42ff", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]"], "product_ndc": "69238-1424", "generic_name": "Vigabatrin", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vigabatrin", "active_ingredients": [{"name": "VIGABATRIN", "strength": "500 mg/1"}], "application_number": "ANDA210042", "marketing_category": "ANDA", "marketing_start_date": "20220627", "listing_expiration_date": "20261231"}