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Cardizem CD - 64455-795-42 - (Diltiazem Hydrochloride)

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Drug Information of Cardizem CD

Product NDC: 64455-795
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: 64455-795
Labeler Name: BTA Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020062
Marketing Category: NDA
Start Marketing Date: 20010411

Package Information of Cardizem CD

Package NDC: 64455-795-42
Package Description: 90 CAPSULE in 1 BOTTLE, PLASTIC (64455-795-42)

NDC Information of Cardizem CD

NDC Code 64455-795-42
Proprietary Name Cardizem CD
Package Description 90 CAPSULE in 1 BOTTLE, PLASTIC (64455-795-42)
Product NDC 64455-795
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 BTA Pharmaceuticals Inc.
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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