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TIAZAC
TIAZAC - 0456-2616-63 - (diltiazem hydrochloride)
Drug Information of TIAZAC
| Product NDC: | 0456-2616 |
| Proprietary Name: | TIAZAC |
| Non Proprietary Name: | diltiazem hydrochloride |
| Active Ingredient(s): | 360 mg/1 & nbsp; diltiazem hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TIAZAC
| Product NDC: | 0456-2616 |
| Labeler Name: | Forest Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020401 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20101225 |
Package Information of TIAZAC
| Package NDC: | 0456-2616-63 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (0456-2616-63) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0456-2616-11) |
NDC Information of TIAZAC
| NDC Code | 0456-2616-63 |
| Proprietary Name | TIAZAC |
| Package Description | 10 BLISTER PACK in 1 CARTON (0456-2616-63) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0456-2616-11) |
| Product NDC | 0456-2616 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | diltiazem hydrochloride |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20101225 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Forest Laboratories, Inc. |
| Substance Name | DILTIAZEM HYDROCHLORIDE |
| Strength Number | 360 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
