| NDC Code | 63304-722-05 |
|---|
| Package Description | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-722-05) |
|---|
| Product NDC | 63304-722 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Diltiazem Hydrochloride |
|---|
| Non-Proprietary Name | Diltiazem Hydrochloride |
|---|
| Dosage Form | CAPSULE, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20181031 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203023 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | DILTIAZEM HYDROCHLORIDE |
|---|
| Strength | 360 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA] |
|---|