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Vasopressin - 63323-302-01 - (VASOPRESSIN)

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Drug Information of Vasopressin

Product NDC: 63323-302
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: 63323-302
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20010717

Package Information of Vasopressin

Package NDC: 63323-302-01
Package Description: 25 VIAL in 1 TRAY (63323-302-01) > 1 mL in 1 VIAL

NDC Information of Vasopressin

NDC Code 63323-302-01
Proprietary Name Vasopressin
Package Description 25 VIAL in 1 TRAY (63323-302-01) > 1 mL in 1 VIAL
Product NDC 63323-302
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VASOPRESSIN
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; SUBCUTANEOUS
Start Marketing Date 20010717
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name APP Pharmaceuticals, LLC
Substance Name VASOPRESSIN
Strength Number 20
Strength Unit [USP'U]/mL
Pharmaceutical Classes

Complete Information of Vasopressin


General Information