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

Drug Name: FACTREL
FDA Application No: (NDA) 018123
Active Ingredient(s): GONADORELIN HYDROCHLORIDE
Company: BAXTER HLTHCARE CORP
Original Approval or Tentative Approval Date: September 30, 1982
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
FACTREL GONADORELIN HYDROCHLORIDEEQ 0.1MG BASE/VIALINJECTABLE; INJECTION Discontinued No None
FACTREL GONADORELIN HYDROCHLORIDEEQ 0.2MG BASE/VIALINJECTABLE; INJECTION Discontinued No None
FACTREL GONADORELIN HYDROCHLORIDEEQ 0.5MG BASE/VIALINJECTABLE; INJECTION Discontinued No None


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