VELOSEF Detail

Drug Name(s):
VELOSEF

FDA Application No.:
NDA 061764

Active Ingredient(s):
CEPHRADINE

Company:
APOTHECON

Original Approval or Tentative Approval Date:
August 18, 1974

Products on Application NDA 061764:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
CEPHRADINE	500MG	CAPSULE; ORAL	Prescription	AB

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last updated on 01-08-2009

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