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Diltiazem Hydrochloride - 54868-4186-0 - (diltiazem hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 54868-4186
Proprietary Name: Diltiazem Hydrochloride
Non Proprietary Name: diltiazem hydrochloride
Active Ingredient(s): 180    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: 54868-4186
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020401
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20000515

Package Information of Diltiazem Hydrochloride

Package NDC: 54868-4186-0
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4186-0)

NDC Information of Diltiazem Hydrochloride

NDC Code 54868-4186-0
Proprietary Name Diltiazem Hydrochloride
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4186-0)
Product NDC 54868-4186
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diltiazem hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20000515
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Physicians Total Care, Inc.
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Diltiazem Hydrochloride


General Information