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Diltiazem Hydrochloride - 0093-5118-05 - (Diltiazem Hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 0093-5118
Proprietary Name: Diltiazem Hydrochloride
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 Diltiazem Hydrochloride

Product NDC: 0093-5118
Labeler Name: TEVA Pharmaceuticals USA Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075116
Marketing Category: ANDA
Start Marketing Date: 19991228

Package Information of Diltiazem Hydrochloride

Package NDC: 0093-5118-05
Package Description: 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5118-05)

NDC Information of Diltiazem Hydrochloride

NDC Code 0093-5118-05
Proprietary Name Diltiazem Hydrochloride
Package Description 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5118-05)
Product NDC 0093-5118
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19991228
Marketing Category Name ANDA
Labeler Name TEVA Pharmaceuticals USA Inc.
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 240
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Diltiazem Hydrochloride


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