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Diltiazem Hydrochloride - 49349-003-02 - (Diltiazem Hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 49349-003
Proprietary Name: Diltiazem Hydrochloride
Non Proprietary Name: Diltiazem Hydrochloride
Active Ingredient(s): 180    mg/1 & nbsp;   Diltiazem Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 49349-003
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074984
Marketing Category: ANDA
Start Marketing Date: 20110803

Package Information of Diltiazem Hydrochloride

Package NDC: 49349-003-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (49349-003-02)

NDC Information of Diltiazem Hydrochloride

NDC Code 49349-003-02
Proprietary Name Diltiazem Hydrochloride
Package Description 30 CAPSULE in 1 BLISTER PACK (49349-003-02)
Product NDC 49349-003
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110803
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Diltiazem Hydrochloride


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