Visitor Monitoring Drug Details: CECLOR
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: CECLOR
FDA Application No: (NDA) 050522
Active Ingredient(s): CEFACLOR
Company: LILLY
Original Approval or Tentative Approval Date: April 4, 1979
Chemical Type: 2 New active ingredient
Review Classification: S Standard review drug
 
Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
CECLOR CEFACLOREQ 125MG BASE/5MLFOR SUSPENSION; ORAL Discontinued No None
CECLOR CEFACLOREQ 250MG BASE/5MLFOR SUSPENSION; ORAL Discontinued No None


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