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Diltiazem Hydrochloride - 68788-8001-1 - (diltiazem)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 68788-8001
Proprietary Name: Diltiazem Hydrochloride
Non Proprietary Name: diltiazem
Active Ingredient(s): 240    mg/1 & nbsp;   diltiazem
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 68788-8001
Labeler Name: Preferred Pharmaceuticals, inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074984
Marketing Category: ANDA
Start Marketing Date: 20110331

Package Information of Diltiazem Hydrochloride

Package NDC: 68788-8001-1
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8001-1)

NDC Information of Diltiazem Hydrochloride

NDC Code 68788-8001-1
Proprietary Name Diltiazem Hydrochloride
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8001-1)
Product NDC 68788-8001
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diltiazem
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110331
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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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