Dicloxacillin Sodium
Dicloxacillin Sodium Capsules, USP250 mg
Approved
Approval ID
33434f66-1d36-4506-9b3d-9755c978d9b2
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 20, 2010
Manufacturers
FDA
Rebel Distributors Corp
DUNS: 118802834
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Dicloxacillin Sodium
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code21695-124
Application NumberANDA061454
Product Classification
M
Marketing Category
C73584
G
Generic Name
Dicloxacillin Sodium
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 10, 2007
FDA Product Classification
INGREDIENTS (5)
DICLOXACILLIN SODIUMActive
Quantity: 250 mg in 1 1
Code: 4HZT2V9KX0
Classification: ACTIB
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
GELATINInactive
Code: 2G86QN327L
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
FD&C BLUE NO. 1Inactive
Code: H3R47K3TBD
Classification: IACT