Visitor Monitoring Drug Details: ZEGERID
 
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Drug Details

Drug Name: ZEGERID
FDA Application No: (NDA) 021636
Active Ingredient(s): OMEPRAZOLE; SODIUM BICARBONATE
Company: SANTARUS
Original Approval or Tentative Approval Date: June 15, 2004
Chemical Type: 34 New dosage form and new combination
Review Classification: S Standard review drug
 
There are no 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
ZEGERID OMEPRAZOLE; SODIUM BICARBONATE20MG/PACKET; 1.68GM/PACKETFOR SUSPENSION; ORAL Prescription No None
ZEGERID OMEPRAZOLE; SODIUM BICARBONATE40MG/PACKET; 1.68GM/PACKETFOR SUSPENSION; ORAL Prescription Yes None


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