Product NDC: | 55154-4251 |
Proprietary Name: | Cardizem |
Non Proprietary Name: | diltiazem hydrochloride |
Active Ingredient(s): | 240 mg/1 & nbsp; diltiazem hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-4251 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020062 |
Marketing Category: | NDA |
Start Marketing Date: | 20010411 |
Package NDC: | 55154-4251-0 |
Package Description: | 10 BLISTER PACK in 1 BAG (55154-4251-0) > 1 CAPSULE in 1 BLISTER PACK |
NDC Code | 55154-4251-0 |
Proprietary Name | Cardizem |
Package Description | 10 BLISTER PACK in 1 BAG (55154-4251-0) > 1 CAPSULE in 1 BLISTER PACK |
Product NDC | 55154-4251 |
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 | Cardinal Health |
Substance Name | DILTIAZEM HYDROCHLORIDE |
Strength Number | 240 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |