Sumatriptan Succinate
Sumatriptan succinate
Approved
Approval ID
68daf82a-334e-43ca-b4bb-5c66a82f52c8
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 1, 2020
Manufacturers
FDA
Proficient Rx LP
DUNS: 079196022
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 Code63187-049
Application NumberANDA076847
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateFebruary 1, 2020
Generic NameSumatriptan Succinate
INGREDIENTS (10)
sumatriptan succinateActive
Quantity: 50 mg in 1 1
Code: J8BDZ68989
Classification: ACTIM
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Code: 7SEV7J4R1U
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LACTOSE MONOHYDRATEInactive
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Classification: IACT
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Code: OP1R32D61U
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Code: 70097M6I30
Classification: IACT
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Code: 3OWL53L36A
Classification: IACT
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Classification: IACT
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Code: XHX3C3X673
Classification: IACT