Product NDC: | 52533-103 |
Proprietary Name: | Diltiazem HCl |
Non Proprietary Name: | Diltiazem HCl |
Active Ingredient(s): | 1 mg/mL & nbsp; Diltiazem HCl |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52533-103 |
Labeler Name: | Cantrell Drug Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110930 |
Package NDC: | 52533-103-13 |
Package Description: | 125 mL in 1 BAG (52533-103-13) |
NDC Code | 52533-103-13 |
Proprietary Name | Diltiazem HCl |
Package Description | 125 mL in 1 BAG (52533-103-13) |
Product NDC | 52533-103 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Diltiazem HCl |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20110930 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Cantrell Drug Company |
Substance Name | DILTIAZEM HYDROCHLORIDE |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |