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VinCRIStine Sulfate - 61703-309-25 - (VINCRISTINE SULFATE)

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Drug Information of VinCRIStine Sulfate

Product NDC: 61703-309
Proprietary Name: VinCRIStine Sulfate
Non Proprietary Name: VINCRISTINE SULFATE
Active Ingredient(s): 1    mg/mL & nbsp;   VINCRISTINE SULFATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of VinCRIStine Sulfate

Product NDC: 61703-309
Labeler Name: Hospira Worldwide, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071484
Marketing Category: ANDA
Start Marketing Date: 19880419

Package Information of VinCRIStine Sulfate

Package NDC: 61703-309-25
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON (61703-309-25) > 2 mL in 1 VIAL, SINGLE-USE

NDC Information of VinCRIStine Sulfate

NDC Code 61703-309-25
Proprietary Name VinCRIStine Sulfate
Package Description 1 VIAL, SINGLE-USE in 1 CARTON (61703-309-25) > 2 mL in 1 VIAL, SINGLE-USE
Product NDC 61703-309
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VINCRISTINE SULFATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19880419
Marketing Category Name ANDA
Labeler Name Hospira Worldwide, Inc.
Substance Name VINCRISTINE SULFATE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Vinca Alkaloid [EPC],Vinca Alkaloids [Chemical/Ingredient]

Complete Information of VinCRIStine Sulfate


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