General MedicationsINJECTIONGeneric
VELOSEF
CEPHRADINE
Standard Dose
1GM/VIAL
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary
Approval overview VELOSEF is listed in Drugs@FDA under application 061976 (ANDA).
Marketing status: Discontinued Active ingredient CEPHRADINE Form and strength INJECTABLE;INJECTION - 1GM/VIAL Sponsor APOTHECON Submission history Latest submission status date: 1977-02-09 00:00:00.
Structured Monograph
Clinical summary
Approval overview VELOSEF is listed in Drugs@FDA under application 061976 (ANDA). Marketing status: Discontinued Active ingredient CEPHRADINE Form and strength INJECTABLE;INJECTION - 1GM/VIAL Sponsor APOTHECON Submission history Latest submission status date: 1977-02-09 00:00:00. Submission type: ORIG.
Monitoring
- • Marketing status: Discontinued
Interaction Notes
- No interaction notes stored yet.