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Desmopressin acetate - 0703-5054-01 - (Desmopressin acetate)

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Drug Information of Desmopressin acetate

Product NDC: 0703-5054
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): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Desmopressin acetate

Product NDC: 0703-5054
Labeler Name: Teva Parenteral Medicines, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074888
Marketing Category: ANDA
Start Marketing Date: 19971101

Package Information of Desmopressin acetate

Package NDC: 0703-5054-01
Package Description: 1 VIAL in 1 CARTON (0703-5054-01) > 10 mL in 1 VIAL

NDC Information of Desmopressin acetate

NDC Code 0703-5054-01
Proprietary Name Desmopressin acetate
Package Description 1 VIAL in 1 CARTON (0703-5054-01) > 10 mL in 1 VIAL
Product NDC 0703-5054
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desmopressin acetate
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19971101
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, 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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