Spectramast
SPECTRAMAST LC
Approved
Approval ID
35017960-b3c3-4e05-803c-e4a8b7009d83
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 Code54771-5279
Application NumberNADA141238
Product Classification
M
Marketing Category
C73593
G
Generic Name
ceftiofur hydrochloride
Product Specifications
Route of AdministrationINTRAMAMMARY
Effective DateMarch 26, 2025
FDA Product Classification
INGREDIENTS (3)
APRICOT KERNEL OIL PEG-6 ESTERSInactive
Code: DRG3KJZ1TJ
Classification: IACT
MICROCRYSTALLINE WAXInactive
Quantity: 700 mg in 10 mL
Code: XOF597Q3KY
Classification: IACT
CEFTIOFUR HYDROCHLORIDEActive
Quantity: 125 mg in 10 mL
Code: 6822A07436
Classification: ACTIM