| NDC Code | 68682-372-90 |
|---|
| Package Description | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68682-372-90) |
|---|
| Product NDC | 68682-372 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Diltiazem Hydrochloride |
|---|
| Proprietary Name Suffix | Extended Release |
|---|
| Non-Proprietary Name | Diltiazem Hydrochloride |
|---|
| Dosage Form | CAPSULE, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20140820 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA020401 |
|---|
| Manufacturer | Oceanside Pharmaceuticals |
|---|
| Substance Name | DILTIAZEM HYDROCHLORIDE |
|---|
| Strength | 420 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA] |
|---|