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Diltiazem Hydrochloride - 55390-374-10 - (Diltiazem Hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 55390-374
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, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 55390-374
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074617
Marketing Category: ANDA
Start Marketing Date: 20090309

Package Information of Diltiazem Hydrochloride

Package NDC: 55390-374-10
Package Description: 10 VIAL in 1 BOX (55390-374-10) > 10 mL in 1 VIAL

NDC Information of Diltiazem Hydrochloride

NDC Code 55390-374-10
Proprietary Name Diltiazem Hydrochloride
Package Description 10 VIAL in 1 BOX (55390-374-10) > 10 mL in 1 VIAL
Product NDC 55390-374
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20090309
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
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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