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Cardizem CD
Cardizem CD - 0187-0795-49 - (Diltiazem Hydrochloride)
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: | 0187-0795-49 |
| Package Description: | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0187-0795-49) > 10 CAPSULE in 1 BLISTER PACK |
NDC Information of Cardizem CD
| NDC Code | 0187-0795-49 |
| Proprietary Name | Cardizem CD |
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0187-0795-49) > 10 CAPSULE in 1 BLISTER PACK |
| 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] |
