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Diltiazem Hydrochloride - 0904-6149-61 - (Diltiazem Hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 0904-6149
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: 0904-6149
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074984
Marketing Category: ANDA
Start Marketing Date: 20100512

Package Information of Diltiazem Hydrochloride

Package NDC: 0904-6149-61
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0904-6149-61)

NDC Information of Diltiazem Hydrochloride

NDC Code 0904-6149-61
Proprietary Name Diltiazem Hydrochloride
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0904-6149-61)
Product NDC 0904-6149
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100512
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
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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