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Desmopressin Acetate - 54868-5602-0 - (Desmopressin Acetate)

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Drug Information of Desmopressin Acetate

Product NDC: 54868-5602
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: 54868-5602
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074830
Marketing Category: ANDA
Start Marketing Date: 20060522

Package Information of Desmopressin Acetate

Package NDC: 54868-5602-0
Package Description: 1 BOTTLE, PUMP in 1 CARTON (54868-5602-0) > 5 mL in 1 BOTTLE, PUMP

NDC Information of Desmopressin Acetate

NDC Code 54868-5602-0
Proprietary Name Desmopressin Acetate
Package Description 1 BOTTLE, PUMP in 1 CARTON (54868-5602-0) > 5 mL in 1 BOTTLE, PUMP
Product NDC 54868-5602
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desmopressin Acetate
Dosage Form Name SOLUTION
Route Name NASAL
Start Marketing Date 20060522
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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