FDA Product

Spectramast DC

Product approved by U.S. Food and Drug Administration (US)

Basic Information

Product Name

Spectramast DC

FDA Product Code

54771-5278

Regulatory Information

NDC Product Code

54771-5278

Application Number

NADA141239

Marketing Category

C73593

Effective Date

March 26, 2025

Territorial Authority

USA

FDA Title

SPECTRAMAST DC

Labeling Type

PRESCRIPTION ANIMAL DRUG LABEL

Version Number

5

Company Information

ManufacturerZoetis Inc.

DUNS Number

828851555

Active Ingredients

MICROCRYSTALLINE WAX

Code: XOF597Q3KY

Class Code: IACT

CEFTIOFUR HYDROCHLORIDE

Quantity: 500 mg in 10 mL

Code: 6822A07436

Class Code: ACTIM

Active Moieties

CEFTIOFUR

Code: 83JL932I1C

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