Spectramast
SPECTRAMAST DC
Approved
Approval ID
eea5a063-8583-4f9b-8377-aa4c7e9fd302
Product Type
PRESCRIPTION ANIMAL DRUG LABEL
Effective Date
Mar 26, 2025
Manufacturers
FDA
Zoetis Inc.
DUNS: 828851555
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
ceftiofur hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54771-5278
Application NumberNADA141239
Product Classification
M
Marketing Category
C73593
G
Generic Name
ceftiofur hydrochloride
Product Specifications
Route of AdministrationINTRAMAMMARY
Effective DateMarch 26, 2025
FDA Product Classification
INGREDIENTS (2)
MICROCRYSTALLINE WAXInactive
Code: XOF597Q3KY
Classification: IACT
CEFTIOFUR HYDROCHLORIDEActive
Quantity: 500 mg in 10 mL
Code: 6822A07436
Classification: ACTIM