| NDC Code | 43353-888-17 |
|---|
| Package Description | 6030 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43353-888-17) |
|---|
| Product NDC | 43353-888 |
|---|
| 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 | 20090925 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA020401 |
|---|
| Manufacturer | Aphena Pharma Solutions - Tennessee, LLC |
|---|
| Substance Name | DILTIAZEM HYDROCHLORIDE |
|---|
| Strength | 120 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
|---|