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Diltiazem Hydrochloride - 63629-4141-2 - (diltiazem hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 63629-4141
Proprietary Name: Diltiazem Hydrochloride
Non Proprietary Name: diltiazem hydrochloride
Active Ingredient(s): 120    mg/1 & nbsp;   diltiazem hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 63629-4141
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075124
Marketing Category: ANDA
Start Marketing Date: 20101102

Package Information of Diltiazem Hydrochloride

Package NDC: 63629-4141-2
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-4141-2)

NDC Information of Diltiazem Hydrochloride

NDC Code 63629-4141-2
Proprietary Name Diltiazem Hydrochloride
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-4141-2)
Product NDC 63629-4141
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diltiazem hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20101102
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Diltiazem Hydrochloride


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