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diltiazem hydrochloride - 0258-3691-90 - (diltiazem hydrochloride)

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Drug Information of diltiazem hydrochloride

Product NDC: 0258-3691
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: 0258-3691
Labeler Name: Forest Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020401
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20090925

Package Information of diltiazem hydrochloride

Package NDC: 0258-3691-90
Package Description: 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0258-3691-90)

NDC Information of diltiazem hydrochloride

NDC Code 0258-3691-90
Proprietary Name diltiazem hydrochloride
Package Description 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0258-3691-90)
Product NDC 0258-3691
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diltiazem hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090925
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Forest Laboratories, Inc.
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


General Information