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Diltiazem Hydrochloride - 0641-6013-10 - (Diltiazem Hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 0641-6013
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: 0641-6013
Labeler Name: West-ward Pharmaceutical Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078538
Marketing Category: ANDA
Start Marketing Date: 20081217

Package Information of Diltiazem Hydrochloride

Package NDC: 0641-6013-10
Package Description: 10 VIAL in 1 CARTON (0641-6013-10) > 5 mL in 1 VIAL (0641-6013-01)

NDC Information of Diltiazem Hydrochloride

NDC Code 0641-6013-10
Proprietary Name Diltiazem Hydrochloride
Package Description 10 VIAL in 1 CARTON (0641-6013-10) > 5 mL in 1 VIAL (0641-6013-01)
Product NDC 0641-6013
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20081217
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp.
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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