NDC Code | 24979-030-07 |
Package Description | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (24979-030-07) |
Product NDC | 24979-030 |
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 | 20181001 |
Marketing Category Name | ANDA |
Application Number | ANDA205231 |
Manufacturer | TWi Pharmaceuticals, 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] |