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Desmopressin Acetate - 55566-5040-1 - (desmopressin acetate)

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Drug Information of Desmopressin Acetate

Product NDC: 55566-5040
Proprietary Name: Desmopressin Acetate
Non Proprietary Name: desmopressin acetate
Active Ingredient(s): 4    ug/mL & nbsp;   desmopressin acetate
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Desmopressin Acetate

Product NDC: 55566-5040
Labeler Name: Ferring Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018938
Marketing Category: NDA
Start Marketing Date: 19991026

Package Information of Desmopressin Acetate

Package NDC: 55566-5040-1
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (55566-5040-1) > 10 mL in 1 VIAL, MULTI-DOSE (55566-5040-0)

NDC Information of Desmopressin Acetate

NDC Code 55566-5040-1
Proprietary Name Desmopressin Acetate
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (55566-5040-1) > 10 mL in 1 VIAL, MULTI-DOSE (55566-5040-0)
Product NDC 55566-5040
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name desmopressin acetate
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19991026
Marketing Category Name NDA
Labeler Name Ferring Pharmaceuticals Inc.
Substance Name DESMOPRESSIN ACETATE
Strength Number 4
Strength Unit ug/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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