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Vasopressin - 0517-0510-25 - (Vasopressin)

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Drug Information of Vasopressin

Product NDC: 0517-0510
Proprietary Name: Vasopressin
Non Proprietary Name: Vasopressin
Active Ingredient(s): 20    [USP'U]/mL & nbsp;   Vasopressin
Administration Route(s): INTRAMUSCULAR; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Vasopressin

Product NDC: 0517-0510
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19921001

Package Information of Vasopressin

Package NDC: 0517-0510-25
Package Description: 25 VIAL, MULTI-DOSE in 1 CARTON (0517-0510-25) > .5 mL in 1 VIAL, MULTI-DOSE

NDC Information of Vasopressin

NDC Code 0517-0510-25
Proprietary Name Vasopressin
Package Description 25 VIAL, MULTI-DOSE in 1 CARTON (0517-0510-25) > .5 mL in 1 VIAL, MULTI-DOSE
Product NDC 0517-0510
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Vasopressin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; SUBCUTANEOUS
Start Marketing Date 19921001
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name American Regent, Inc.
Substance Name ARGIPRESSIN
Strength Number 20
Strength Unit [USP'U]/mL
Pharmaceutical Classes

Complete Information of Vasopressin


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