| NDC Code | 0456-2612-00 |
|---|
| Package Description | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0456-2612-00) |
|---|
| Product NDC | 0456-2612 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Tiazac |
|---|
| Proprietary Name Suffix | Extended Release |
|---|
| Non-Proprietary Name | Diltiazem Hydrochloride |
|---|
| Dosage Form | CAPSULE, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20101225 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA020401 |
|---|
| Manufacturer | Forest Laboratories, Inc. |
|---|
| Substance Name | DILTIAZEM HYDROCHLORIDE |
|---|
| Strength | 120 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
|---|