NDC Code | 0615-8381-39 |
Package Description | 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0615-8381-39) |
Product NDC | 0615-8381 |
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 | 20190614 |
Marketing Category Name | ANDA |
Application Number | ANDA208783 |
Manufacturer | NCS HealthCare of KY, LLC dba Vangard Labs |
Substance Name | DILTIAZEM HYDROCHLORIDE |
Strength | 240 |
Strength Unit | mg/1 |
Pharmacy Classes | Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA] |