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Diltiazem Hydrochloride - 0409-1171-01 - (Diltiazem Hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 0409-1171
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: 0409-1171
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074941
Marketing Category: ANDA
Start Marketing Date: 20120410

Package Information of Diltiazem Hydrochloride

Package NDC: 0409-1171-01
Package Description: 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1171-01) > 5 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Diltiazem Hydrochloride

NDC Code 0409-1171-01
Proprietary Name Diltiazem Hydrochloride
Package Description 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1171-01) > 5 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0409-1171
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120410
Marketing Category Name ANDA
Labeler Name Hospira, 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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