DDAVP - 0075-2452-01 - (desmopressin acetate)

Alphabetical Index


Drug Information of DDAVP

Product NDC: 0075-2452
Proprietary Name: DDAVP
Non Proprietary Name: desmopressin acetate
Active Ingredient(s): .1    mg/mL & nbsp;   desmopressin acetate
Administration Route(s): NASAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of DDAVP

Product NDC: 0075-2452
Labeler Name: sanofi-aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017922
Marketing Category: NDA
Start Marketing Date: 19780221

Package Information of DDAVP

Package NDC: 0075-2452-01
Package Description: 5 mL in 1 BOTTLE, SPRAY (0075-2452-01)

NDC Information of DDAVP

NDC Code 0075-2452-01
Proprietary Name DDAVP
Package Description 5 mL in 1 BOTTLE, SPRAY (0075-2452-01)
Product NDC 0075-2452
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name desmopressin acetate
Dosage Form Name SOLUTION
Route Name NASAL
Start Marketing Date 19780221
Marketing Category Name NDA
Labeler Name sanofi-aventis U.S. LLC
Substance Name DESMOPRESSIN ACETATE
Strength Number .1
Strength Unit mg/mL
Pharmaceutical Classes Factor VIII Activator [EPC],Increased Coagulation Factor VIII Activity [PE],Increased Coagulation Factor VIII Concentration [PE],Vasopressin Analog [EPC],Vasopressins [Chemical/Ingredient]

Complete Information of DDAVP


General Information