vigafyde
Generic: vigabatrin
Labeler: upsher-smith laboratories, llcDrug Facts
Product Profile
Brand Name
vigafyde
Generic Name
vigabatrin
Labeler
upsher-smith laboratories, llc
Dosage Form
SOLUTION
Routes
Active Ingredients
vigabatrin 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
80789-003
Product ID
80789-003_43aeb38a-b4ee-47ed-8239-c488b074f1c9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA217684
Listing Expiration
2027-12-31
Marketing Start
2024-06-18
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
80789003
Hyphenated Format
80789-003
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
vigafyde (source: ndc)
Generic Name
vigabatrin (source: ndc)
Application Number
NDA217684 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (80789-003-15) / 150 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43aeb38a-b4ee-47ed-8239-c488b074f1c9", "openfda": {"nui": ["N0000175753"], "unii": ["GR120KRT6K"], "rxcui": ["2685217", "2685223"], "spl_set_id": ["8d3d6316-33ab-41e8-9485-4495c218be56"], "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 (80789-003-15) / 150 mL in 1 BOTTLE", "package_ndc": "80789-003-15", "marketing_start_date": "20240826"}], "brand_name": "VIGAFYDE", "product_id": "80789-003_43aeb38a-b4ee-47ed-8239-c488b074f1c9", "dosage_form": "SOLUTION", "pharm_class": ["Anti-epileptic Agent [EPC]"], "product_ndc": "80789-003", "generic_name": "vigabatrin", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VIGAFYDE", "active_ingredients": [{"name": "VIGABATRIN", "strength": "100 mg/mL"}], "application_number": "NDA217684", "marketing_category": "NDA", "marketing_start_date": "20240618", "listing_expiration_date": "20271231"}