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Diltiazem Hydrochloride - 17478-837-10 - (Diltiazem Hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 17478-837
Proprietary Name: Diltiazem Hydrochloride
Non Proprietary Name: Diltiazem Hydrochloride
Active Ingredient(s): 5    mg/mL & nbsp;   Diltiazem Hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 17478-837
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075086
Marketing Category: ANDA
Start Marketing Date: 20130322

Package Information of Diltiazem Hydrochloride

Package NDC: 17478-837-10
Package Description: 10 VIAL, SINGLE-USE in 1 CARTON (17478-837-10) > 10 mL in 1 VIAL, SINGLE-USE

NDC Information of Diltiazem Hydrochloride

NDC Code 17478-837-10
Proprietary Name Diltiazem Hydrochloride
Package Description 10 VIAL, SINGLE-USE in 1 CARTON (17478-837-10) > 10 mL in 1 VIAL, SINGLE-USE
Product NDC 17478-837
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20130322
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Diltiazem Hydrochloride


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