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Cardizem LA - 0074-3061-90 - (Diltiazem Hydrochloride)

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Drug Information of Cardizem LA

Product NDC: 0074-3061
Proprietary Name: Cardizem LA
Non Proprietary Name: Diltiazem Hydrochloride
Active Ingredient(s): 180    mg/1 & nbsp;   Diltiazem Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Cardizem LA

Product NDC: 0074-3061
Labeler Name: AbbVie Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021392
Marketing Category: NDA
Start Marketing Date: 20101225

Package Information of Cardizem LA

Package NDC: 0074-3061-90
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0074-3061-90)

NDC Information of Cardizem LA

NDC Code 0074-3061-90
Proprietary Name Cardizem LA
Package Description 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0074-3061-90)
Product NDC 0074-3061
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20101225
Marketing Category Name NDA
Labeler Name AbbVie 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 Cardizem LA


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