NDC Code | 68071-3079-3 |
Package Description | 30 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (68071-3079-3) |
Product NDC | 68071-3079 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Diltiazem Hydrochloride |
Proprietary Name Suffix | Extended Release |
Non-Proprietary Name | Diltiazem Hydrochloride |
Dosage Form | CAPSULE, COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 19991220 |
Marketing Category Name | ANDA |
Application Number | ANDA074984 |
Manufacturer | NuCare Pharmaceuticals, Inc. |
Substance Name | DILTIAZEM HYDROCHLORIDE |
Strength | 240 |
Strength Unit | mg/1 |
Pharmacy Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |