Sumatriptan
Sumatriptan 100mg Tablet
Approved
Approval ID
f1a118cf-2179-572a-e053-2995a90acbb0
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 12, 2023
Manufacturers
FDA
Advanced Rx Pharmacy of Tennessee, LLC
DUNS: 117023142
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Sumatriptan
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code80425-0224
Application NumberANDA078327
Product Classification
M
Marketing Category
C73584
G
Generic Name
Sumatriptan
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 12, 2023
FDA Product Classification
INGREDIENTS (1)
SUMATRIPTAN SUCCINATEActive
Quantity: 100 mg in 1 1
Code: J8BDZ68989
Classification: ACTIM