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Diltiazem Hydrochloride - 49349-557-20 - (DILTIAZEM HYDROCHLORIDE)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 49349-557
Proprietary Name: Diltiazem Hydrochloride
Non Proprietary Name: DILTIAZEM HYDROCHLORIDE
Active Ingredient(s): 30    mg/1 & nbsp;   DILTIAZEM HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 49349-557
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074185
Marketing Category: ANDA
Start Marketing Date: 20120831

Package Information of Diltiazem Hydrochloride

Package NDC: 49349-557-20
Package Description: 100 TABLET in 1 CANISTER (49349-557-20)

NDC Information of Diltiazem Hydrochloride

NDC Code 49349-557-20
Proprietary Name Diltiazem Hydrochloride
Package Description 100 TABLET in 1 CANISTER (49349-557-20)
Product NDC 49349-557
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DILTIAZEM HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120831
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Diltiazem Hydrochloride


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