Package 0245-6001-11
Brand: vigadrone
Generic: vigabatrinPackage Facts
Identity
Package NDC
0245-6001-11
Digits Only
0245600111
Product NDC
0245-6001
Description
1 BOTTLE in 1 CARTON (0245-6001-11) / 100 TABLET in 1 BOTTLE
Marketing
Marketing Status
Brand
vigadrone
Generic
vigabatrin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2734e899-4ddc-836c-e063-6294a90a128f", "openfda": {"nui": ["N0000175753"], "unii": ["GR120KRT6K"], "rxcui": ["199521", "2642353"], "spl_set_id": ["01f7f049-78c2-47c2-a66e-ec662ba48a98"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0245-6001-11) / 100 TABLET in 1 BOTTLE", "package_ndc": "0245-6001-11", "marketing_start_date": "20230630"}], "brand_name": "VIGADRONE", "product_id": "0245-6001_2734e899-4ddc-836c-e063-6294a90a128f", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]"], "product_ndc": "0245-6001", "generic_name": "Vigabatrin", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VIGADRONE", "active_ingredients": [{"name": "VIGABATRIN", "strength": "500 mg/1"}], "application_number": "ANDA214749", "marketing_category": "ANDA", "marketing_start_date": "20230629", "listing_expiration_date": "20261231"}