ECONAZOLE NITRATE 1% / NIACINAMIDE 4%
ECONAZOLE NITRATE 1% / NIACINAMIDE 4%
Approved
Approval ID
895613a0-68c6-2f38-e053-2995a90af107
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 20, 2019
Manufacturers
FDA
Sincerus Florida, LLC
DUNS: 080105003
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
ECONAZOLE NITRATE 1% / NIACINAMIDE 4%
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72934-2073
Product Classification
G
Generic Name
ECONAZOLE NITRATE 1% / NIACINAMIDE 4%
Product Specifications
Route of AdministrationTOPICAL
Effective DateMay 20, 2019
FDA Product Classification
INGREDIENTS (2)
ECONAZOLE NITRATEActive
Quantity: 1 g in 100 g
Code: H438WYN10E
Classification: ACTIB
NIACINAMIDEActive
Quantity: 4 g in 100 g
Code: 25X51I8RD4
Classification: ACTIB