# Implantation or Injectable Dosage Form New Animal Drugs; Ceftiofur Hydrochloride Sterile Suspension
> **Food and Drug Administration** · Final rule. · Published 1998-10-06 · Effective 1998-10-06 · 63 FR 53578
## Document
- **Document number:** 98-26650
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 63 FR 53578
- **CFR reference:** 21 CFR 522
- **Publication date:** 1998-10-06
- **Effective date:** 1998-10-06
## Abstract

The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of two supplemental new animal drug applications (NADA's) filed by Pharmacia & Upjohn Co. One supplemental NADA provides for veterinary prescription use of ceftiofur hydrochloride sterile suspension for intramuscular or subcutaneous injection in cattle for treatment of bovine respiratory disease and acute bovine interdigital necrobacillosis. The second supplemental NADA provides for a revised label warning against use in veal calves.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/1998/10/06/98-26650/implantation-or-injectable-dosage-form-new-animal-drugs-ceftiofur-hydrochloride-sterile-suspension)
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