sumatriptan succinate
Sumatriptan Succinate Injection
Approved
Approval ID
05adc16c-4c2b-46f0-b810-bb18d4106dc5
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 4, 2009
Manufacturers
FDA
JHP Pharmaceuticals LLC
DUNS: 804894611
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 Code42023-121
Application NumberANDA077871
Product Classification
M
Marketing Category
C73584
G
Generic Name
sumatriptan succinate
Product Specifications
Route of AdministrationSUBCUTANEOUS
Effective DateSeptember 4, 2009
FDA Product Classification
INGREDIENTS (3)
sumatriptan succinateActive
Quantity: 6 mg in 0.5 mL
Code: J8BDZ68989
Classification: ACTIM
sodium chlorideInactive
Quantity: 3.5 mg in 0.5 mL
Code: 451W47IQ8X
Classification: IACT
waterInactive
Code: 059QF0KO0R
Classification: IACT