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Cardizem LA
Cardizem LA - 0074-3069-90 - (Diltiazem Hydrochloride)
Drug Information of Cardizem LA
| Product NDC: | 0074-3069 |
| Proprietary Name: | Cardizem LA |
| Non Proprietary Name: | Diltiazem Hydrochloride |
| Active Ingredient(s): | 420 mg/1 & nbsp; Diltiazem Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cardizem LA
| Product NDC: | 0074-3069 |
| Labeler Name: | AbbVie Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021392 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101225 |
Package Information of Cardizem LA
| Package NDC: | 0074-3069-90 |
| Package Description: | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0074-3069-90) |
NDC Information of Cardizem LA
| NDC Code | 0074-3069-90 |
| Proprietary Name | Cardizem LA |
| Package Description | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0074-3069-90) |
| Product NDC | 0074-3069 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diltiazem Hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20101225 |
| Marketing Category Name | NDA |
| Labeler Name | AbbVie Inc. |
| Substance Name | DILTIAZEM HYDROCHLORIDE |
| Strength Number | 420 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
