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Diltiazem Hydrochloride - 47335-678-81 - (Diltiazem Hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 47335-678
Proprietary Name: Diltiazem Hydrochloride
Non Proprietary Name: Diltiazem Hydrochloride
Active Ingredient(s): 300    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: 47335-678
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090492
Marketing Category: ANDA
Start Marketing Date: 20111031

Package Information of Diltiazem Hydrochloride

Package NDC: 47335-678-81
Package Description: 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-678-81)

NDC Information of Diltiazem Hydrochloride

NDC Code 47335-678-81
Proprietary Name Diltiazem Hydrochloride
Package Description 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-678-81)
Product NDC 47335-678
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20111031
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Diltiazem Hydrochloride


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