Package 59651-367-01

Brand: vigabatrin

Generic: vigabatrin
NDC Package

Package Facts

Identity

Package NDC 59651-367-01
Digits Only 5965136701
Product NDC 59651-367
Product ID 59651-367_42eb5d5d-049e-4291-bab0-12d3369cba8c
Description

1 BOTTLE in 1 CARTON (59651-367-01) / 100 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2022-05-10
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": "42eb5d5d-049e-4291-bab0-12d3369cba8c", "openfda": {"nui": ["N0000175753"], "upc": ["0359651367018"], "unii": ["GR120KRT6K"], "rxcui": ["199521"], "spl_set_id": ["4aaea88b-e0fd-45e3-bb02-604bf8ee9b5b"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (59651-367-01)  / 100 TABLET in 1 BOTTLE", "package_ndc": "59651-367-01", "marketing_start_date": "20220510"}], "brand_name": "Vigabatrin", "product_id": "59651-367_42eb5d5d-049e-4291-bab0-12d3369cba8c", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]"], "product_ndc": "59651-367", "generic_name": "Vigabatrin", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vigabatrin", "active_ingredients": [{"name": "VIGABATRIN", "strength": "500 mg/1"}], "application_number": "ANDA215601", "marketing_category": "ANDA", "marketing_start_date": "20220510", "listing_expiration_date": "20261231"}