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Cardizem CD
Cardizem CD - 64455-796-42 - (Diltiazem Hydrochloride)
Drug Information of Cardizem CD
| Product NDC: | 64455-796 |
| Proprietary Name: | Cardizem CD |
| Non Proprietary Name: | Diltiazem Hydrochloride |
| Active Ingredient(s): | 180 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: | 64455-796 |
| 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: | 64455-796-42 |
| Package Description: | 90 CAPSULE in 1 BOTTLE, PLASTIC (64455-796-42) |
NDC Information of Cardizem CD
| NDC Code | 64455-796-42 |
| Proprietary Name | Cardizem CD |
| Package Description | 90 CAPSULE in 1 BOTTLE, PLASTIC (64455-796-42) |
| Product NDC | 64455-796 |
| 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 | 180 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
