VELOSEF '250' Detail

Drug Name(s):
VELOSEF '250'

FDA Application No.:
NDA 061763

Active Ingredient(s):
CEPHRADINE

Company:
APOTHECON

Original Approval or Tentative Approval Date:
July 8, 1987

Products on Application NDA 061763:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
CEPHRADINE	250MG/5ML	FOR SUSPENSION; ORAL	Prescription	AB

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January 2009

VELOSEF '250' Detail

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