Sumatriptan Succinate
SUMATRIPTAN SUCCINATE tablet, film coated
Approved
Approval ID
94d644b9-9ad1-4c21-9c88-c39796b3e3e6
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 27, 2009
Manufacturers
FDA
Stat Rx USA
DUNS: 786036330
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Sumatriptan Succinate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code16590-300
Application NumberNDA020132
Product Classification
M
Marketing Category
C73594
G
Generic Name
Sumatriptan Succinate
Product Specifications
Route of AdministrationORAL
Effective DateOctober 27, 2009
FDA Product Classification
INGREDIENTS (1)
SUMATRIPTAN SUCCINATEActive
Quantity: 100 mg in 1 1
Code: J8BDZ68989
Classification: ACTIB