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Diltiazem Hydrochloride - 10019-510-01 - (Diltiazem Hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 10019-510
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: 10019-510
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078538
Marketing Category: ANDA
Start Marketing Date: 20100713

Package Information of Diltiazem Hydrochloride

Package NDC: 10019-510-01
Package Description: 10 VIAL, SINGLE-DOSE in 1 PACKAGE (10019-510-01) > 5 mL in 1 VIAL, SINGLE-DOSE (10019-510-79)

NDC Information of Diltiazem Hydrochloride

NDC Code 10019-510-01
Proprietary Name Diltiazem Hydrochloride
Package Description 10 VIAL, SINGLE-DOSE in 1 PACKAGE (10019-510-01) > 5 mL in 1 VIAL, SINGLE-DOSE (10019-510-79)
Product NDC 10019-510
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20100713
Marketing Category Name ANDA
Labeler Name Baxter Healthcare Corporation
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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