Visitor Monitoring Drug Details: PAMIDRONATE DISODIUM
 
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Drug Details

Drug Name: PAMIDRONATE DISODIUM
FDA Application No: (ANDA) 076153
Active Ingredient(s): PAMIDRONATE DISODIUM
Company: TEVA PARENTERAL
Original Approval or Tentative Approval Date: March 27, 2002
 
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
PAMIDRONATE DISODIUM PAMIDRONATE DISODIUM30MG /10ML(3MG/ML)INJECTABLE; INJECTION Prescription No AP
PAMIDRONATE DISODIUM PAMIDRONATE DISODIUM90MG /10ML(9MG/ML)INJECTABLE; INJECTION Prescription No AP


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