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Tiazac Extended Release - 55154-4606-9 - (diltiazem hydrochloride)

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Drug Information of Tiazac Extended Release

Product NDC: 55154-4606
Proprietary Name: Tiazac Extended Release
Non Proprietary Name: diltiazem hydrochloride
Active Ingredient(s): 240    mg/1 & nbsp;   diltiazem hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Tiazac Extended Release

Product NDC: 55154-4606
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020401
Marketing Category: NDA
Start Marketing Date: 20090924

Package Information of Tiazac Extended Release

Package NDC: 55154-4606-9
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55154-4606-9)

NDC Information of Tiazac Extended Release

NDC Code 55154-4606-9
Proprietary Name Tiazac Extended Release
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55154-4606-9)
Product NDC 55154-4606
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diltiazem hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090924
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 240
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Tiazac Extended Release


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