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Diltiazem Hydrochloride - 47335-673-19 - (Diltiazem Hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 47335-673
Proprietary Name: Diltiazem Hydrochloride
Non Proprietary Name: Diltiazem Hydrochloride
Active Ingredient(s): 360    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: 47335-673
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090421
Marketing Category: ANDA
Start Marketing Date: 20101115

Package Information of Diltiazem Hydrochloride

Package NDC: 47335-673-19
Package Description: 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-673-19)

NDC Information of Diltiazem Hydrochloride

NDC Code 47335-673-19
Proprietary Name Diltiazem Hydrochloride
Package Description 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-673-19)
Product NDC 47335-673
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20101115
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 360
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Diltiazem Hydrochloride


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