Package 42799-950-01

Brand: vigabatrin

Generic: vigabatrin
NDC Package

Package Facts

Identity

Package NDC 42799-950-01
Digits Only 4279995001
Product NDC 42799-950
Product ID 42799-950_93ba3894-fd97-4432-9f2d-e7050371e91f
Description

100 TABLET in 1 BOTTLE (42799-950-01)

Marketing

Marketing Status
Marketed Since 2022-06-29
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": "93ba3894-fd97-4432-9f2d-e7050371e91f", "openfda": {"nui": ["N0000175753"], "unii": ["GR120KRT6K"], "rxcui": ["199521"], "spl_set_id": ["93ba3894-fd97-4432-9f2d-e7050371e91f"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Edenbridge Pharmaceuticals LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42799-950-01)", "package_ndc": "42799-950-01", "marketing_start_date": "20220629"}], "brand_name": "Vigabatrin", "product_id": "42799-950_93ba3894-fd97-4432-9f2d-e7050371e91f", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]"], "product_ndc": "42799-950", "generic_name": "Vigabatrin", "labeler_name": "Edenbridge Pharmaceuticals LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vigabatrin", "active_ingredients": [{"name": "VIGABATRIN", "strength": "500 mg/1"}], "application_number": "ANDA215109", "marketing_category": "ANDA", "marketing_start_date": "20220629", "listing_expiration_date": "20261231"}