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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 065418
Company: ANDA REPOSITORY
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
CEFDINIR CEFDINIR 300MG CAPSULE;ORAL Prescription AB No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
07/18/2007 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
08/21/2020 SUPPL-9 Labeling-Package Insert

Label is not available on this site.

05/27/2010 SUPPL-6 Labeling

Label is not available on this site.

07/20/2009 SUPPL-4 Labeling

Label is not available on this site.

09/18/2008 SUPPL-2 Labeling

Label is not available on this site.

02/07/2008 SUPPL-1 Labeling

Label is not available on this site.

CEFDINIR

CAPSULE;ORAL; 300MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
CEFDINIR CEFDINIR 300MG CAPSULE;ORAL Prescription No AB 210220 ALKEM LABS LTD
CEFDINIR CEFDINIR 300MG CAPSULE;ORAL Prescription No AB 065418 ANDA REPOSITORY
CEFDINIR CEFDINIR 300MG CAPSULE;ORAL Prescription No AB 065434 AUROBINDO PHARMA
CEFDINIR CEFDINIR 300MG CAPSULE;ORAL Prescription No AB 065264 LUPIN
CEFDINIR CEFDINIR 300MG CAPSULE;ORAL Prescription No AB 065330 SANDOZ
CEFDINIR CEFDINIR 300MG CAPSULE;ORAL Prescription No AB 065368 TEVA PHARMS
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