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Diltiazem Hydrochloride - 0409-4350-03 - (DILTIAZEM HYDROCHLORIDE)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 0409-4350
Proprietary Name: Diltiazem Hydrochloride
Non Proprietary Name: DILTIAZEM HYDROCHLORIDE
Active Ingredient(s): 100    mg/1 & nbsp;   DILTIAZEM HYDROCHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 0409-4350
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075853
Marketing Category: ANDA
Start Marketing Date: 20111020

Package Information of Diltiazem Hydrochloride

Package NDC: 0409-4350-03
Package Description: 10 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-4350-03) > 1 POWDER, FOR SOLUTION in 1 VIAL, PATENT DELIVERY SYSTEM

NDC Information of Diltiazem Hydrochloride

NDC Code 0409-4350-03
Proprietary Name Diltiazem Hydrochloride
Package Description 10 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-4350-03) > 1 POWDER, FOR SOLUTION in 1 VIAL, PATENT DELIVERY SYSTEM
Product NDC 0409-4350
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DILTIAZEM HYDROCHLORIDE
Dosage Form Name POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20111020
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Diltiazem Hydrochloride


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