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Diltiazem Hydrochloride - 49884-832-11 - (Diltiazem Hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 49884-832
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, COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 49884-832
Labeler Name: Par Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074984
Marketing Category: ANDA
Start Marketing Date: 19991224

Package Information of Diltiazem Hydrochloride

Package NDC: 49884-832-11
Package Description: 30 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (49884-832-11)

NDC Information of Diltiazem Hydrochloride

NDC Code 49884-832-11
Proprietary Name Diltiazem Hydrochloride
Package Description 30 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (49884-832-11)
Product NDC 49884-832
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name CAPSULE, COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19991224
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical, Inc.
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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