Package 69097-964-53
Brand: vigabatrin
Generic: vigabatrinPackage Facts
Identity
Package NDC
69097-964-53
Digits Only
6909796453
Product NDC
69097-964
Description
50 PACKET in 1 CARTON (69097-964-53) / 10 mL in 1 PACKET
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": "4cdad60f-7614-47cb-8594-3c0257e55c28", "openfda": {"nui": ["N0000175753"], "unii": ["GR120KRT6K"], "rxcui": ["250820"], "spl_set_id": ["823cc915-0350-4780-85ed-cd1c338e429d"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Cipla USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 CARTON (69097-964-53) / 10 mL in 1 PACKET", "package_ndc": "69097-964-53", "marketing_start_date": "20191204"}], "brand_name": "VIGABATRIN", "product_id": "69097-964_4cdad60f-7614-47cb-8594-3c0257e55c28", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Anti-epileptic Agent [EPC]"], "product_ndc": "69097-964", "generic_name": "vigabatrin", "labeler_name": "Cipla USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VIGABATRIN", "active_ingredients": [{"name": "VIGABATRIN", "strength": "500 mg/mL"}], "application_number": "ANDA211592", "marketing_category": "ANDA", "marketing_start_date": "20191204", "listing_expiration_date": "20261231"}