Visitor Monitoring Drug Details: GASTROCROM
 
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Drug Details

Drug Name: GASTROCROM
FDA Application No: (NDA) 020479
Active Ingredient(s): CROMOLYN SODIUM
Company: AZUR PHARMA
Original Approval or Tentative Approval Date: February 29, 1996
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Labels are not available
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
GASTROCROM CROMOLYN SODIUM100MG/5MLCONCENTRATE; ORAL Prescription Yes None


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