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Desmopressin Acetate - 0093-7317-01 - (Desmopressin Acetate)

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Drug Information of Desmopressin Acetate

Product NDC: 0093-7317
Proprietary Name: Desmopressin Acetate
Non Proprietary Name: Desmopressin Acetate
Active Ingredient(s): .2    mg/1 & nbsp;   Desmopressin Acetate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Desmopressin Acetate

Product NDC: 0093-7317
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077122
Marketing Category: ANDA
Start Marketing Date: 20060127

Package Information of Desmopressin Acetate

Package NDC: 0093-7317-01
Package Description: 100 TABLET in 1 BOTTLE (0093-7317-01)

NDC Information of Desmopressin Acetate

NDC Code 0093-7317-01
Proprietary Name Desmopressin Acetate
Package Description 100 TABLET in 1 BOTTLE (0093-7317-01)
Product NDC 0093-7317
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desmopressin Acetate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060127
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name DESMOPRESSIN ACETATE
Strength Number .2
Strength Unit mg/1
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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