Visitor Monitoring Drug Details: ACETADOTE
 
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Drug Details

Drug Name: ACETADOTE
FDA Application No: (NDA) 021539
Active Ingredient(s): ACETYLCYSTEINE
Company: CUMBERLAND PHARMS
Original Approval or Tentative Approval Date: January 23, 2004
Chemical Type: 3 New dosage form
Review Classification: P Priority review drug
O Orphan drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ACETADOTE ACETYLCYSTEINE6GM/30ML (200MG/ML)INJECTABLE; INTRAVENOUS Prescription Yes None


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