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
NDC Product Code42023-121
Application NumberANDA077871
Marketing CategoryC73584
Route of AdministrationSUBCUTANEOUS
Effective DateSeptember 4, 2009
Generic Namesumatriptan succinate
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