| NDC Code | 70518-1017-0 |
|---|
| Package Description | 90 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1017-0) |
|---|
| Product NDC | 70518-1017 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Diltiazem Hydrochloride |
|---|
| Proprietary Name Suffix | Extended-release |
|---|
| Non-Proprietary Name | Diltiazem Hydrochloride |
|---|
| Dosage Form | CAPSULE, COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180214 |
|---|
| 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], Cytochrome P450 3A4 Inhibitors [MoA] |
|---|