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Desmopressin Acetate - 55566-5020-1 - (desmopressin acetate)

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Drug Information of Desmopressin Acetate

Product NDC: 55566-5020
Proprietary Name: Desmopressin Acetate
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 Desmopressin Acetate

Product NDC: 55566-5020
Labeler Name: Ferring Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017922
Marketing Category: NDA
Start Marketing Date: 19990810

Package Information of Desmopressin Acetate

Package NDC: 55566-5020-1
Package Description: 1 VIAL in 1 CARTON (55566-5020-1) > 2.5 mL in 1 VIAL

NDC Information of Desmopressin Acetate

NDC Code 55566-5020-1
Proprietary Name Desmopressin Acetate
Package Description 1 VIAL in 1 CARTON (55566-5020-1) > 2.5 mL in 1 VIAL
Product NDC 55566-5020
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name desmopressin acetate
Dosage Form Name SOLUTION
Route Name NASAL
Start Marketing Date 19990810
Marketing Category Name NDA
Labeler Name Ferring Pharmaceuticals Inc.
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 Desmopressin Acetate


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