Product NDC: | 55154-4604 |
Proprietary Name: | Tiazac Extended Release |
Non Proprietary Name: | diltiazem hydrochloride |
Active Ingredient(s): | 120 mg/1 & nbsp; diltiazem hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-4604 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020401 |
Marketing Category: | NDA |
Start Marketing Date: | 20090924 |
Package NDC: | 55154-4604-9 |
Package Description: | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55154-4604-9) |
NDC Code | 55154-4604-9 |
Proprietary Name | Tiazac Extended Release |
Package Description | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55154-4604-9) |
Product NDC | 55154-4604 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | diltiazem hydrochloride |
Dosage Form Name | CAPSULE, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20090924 |
Marketing Category Name | NDA |
Labeler Name | Cardinal Health |
Substance Name | DILTIAZEM HYDROCHLORIDE |
Strength Number | 120 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |