Package 59651-366-50
Brand: vigabatrin
Generic: vigabatrinPackage Facts
Identity
Package NDC
59651-366-50
Digits Only
5965136650
Product NDC
59651-366
Description
50 PACKET in 1 CARTON (59651-366-50) / 1 POWDER, FOR SOLUTION in 1 PACKET (59651-366-07)
Marketing
Marketing Status
Brand
vigabatrin
Generic
vigabatrin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7fa314e2-0506-4061-9058-435a3b5df40d", "openfda": {"nui": ["N0000175753"], "upc": ["0359651366073"], "unii": ["GR120KRT6K"], "rxcui": ["250820"], "spl_set_id": ["c97ce40c-1c5a-479d-9188-5ce03cf7e065"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 CARTON (59651-366-50) / 1 POWDER, FOR SOLUTION in 1 PACKET (59651-366-07)", "package_ndc": "59651-366-50", "marketing_start_date": "20210929"}], "brand_name": "Vigabatrin", "product_id": "59651-366_7fa314e2-0506-4061-9058-435a3b5df40d", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Anti-epileptic Agent [EPC]"], "product_ndc": "59651-366", "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": "ANDA213899", "marketing_category": "ANDA", "marketing_start_date": "20210929", "listing_expiration_date": "20261231"}