ISOXSUPRINE HYDROCHLORIDE
Isoxsuprine Hydrochloride Tablets, USP
Approved
Approval ID
908691b4-7950-4f3e-bbea-ea568fee7ac3
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 2, 2012
Manufacturers
FDA
Vedco dba Valdar
DUNS: 021634266
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
isoxsuprine hydrochloride
PRODUCT DETAILS
NDC Product Code63549-919
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationORAL
Effective DateJanuary 2, 2012
Generic Nameisoxsuprine hydrochloride
INGREDIENTS (5)
isoxsuprine hydrochlorideActive
Quantity: 20 mg in 1 1
Code: V74TEQ36CO
Classification: ACTIB
Lactose MonohydrateInactive
Code: EWQ57Q8I5X
Classification: IACT
Magnesium StearateInactive
Code: 70097M6I30
Classification: IACT
Cellulose, MicrocrystallineInactive
Code: OP1R32D61U
Classification: IACT
Starch, CornInactive
Code: O8232NY3SJ
Classification: IACT