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Cardizem CD - 0187-0795-30 - (Diltiazem Hydrochloride)

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Drug Information of Cardizem CD

Product NDC: 0187-0795
Proprietary Name: Cardizem CD
Non Proprietary Name: Diltiazem Hydrochloride
Active Ingredient(s): 120    mg/1 & nbsp;   Diltiazem Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Cardizem CD

Product NDC: 0187-0795
Labeler Name: Valeant Pharmaceuticals North America LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020062
Marketing Category: NDA
Start Marketing Date: 20010411

Package Information of Cardizem CD

Package NDC: 0187-0795-30
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (0187-0795-30)

NDC Information of Cardizem CD

NDC Code 0187-0795-30
Proprietary Name Cardizem CD
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (0187-0795-30)
Product NDC 0187-0795
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20010411
Marketing Category Name NDA
Labeler Name Valeant Pharmaceuticals North America LLC
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Cardizem CD


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