| NDC Code | 52125-776-23 |
|---|
| Package Description | 180 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (52125-776-23) |
|---|
| Product NDC | 52125-776 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Diltiazem Hydrochlorideextended Release |
|---|
| Proprietary Name Suffix | Extended Release |
|---|
| Non-Proprietary Name | Diltiazem Hydrochloride |
|---|
| Dosage Form | CAPSULE, COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20150722 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA074984 |
|---|
| Manufacturer | REMEDYREPACK INC. |
|---|
| Substance Name | DILTIAZEM HYDROCHLORIDE |
|---|
| Strength | 120 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
|---|