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Diltiazem Hydrochloride - 53808-0612-1 - (DILTIAZEM HYDROCHLORIDE)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 53808-0612
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 53808-0612
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074984
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Diltiazem Hydrochloride

Package NDC: 53808-0612-1
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (53808-0612-1)

NDC Information of Diltiazem Hydrochloride

NDC Code 53808-0612-1
Proprietary Name Diltiazem Hydrochloride
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (53808-0612-1)
Product NDC 53808-0612
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DILTIAZEM HYDROCHLORIDE
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
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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