Product NDC: | 0409-1171 |
Proprietary Name: | Diltiazem Hydrochloride |
Non Proprietary Name: | Diltiazem Hydrochloride |
Active Ingredient(s): | 5 mg/mL & nbsp; Diltiazem Hydrochloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-1171 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074941 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120410 |
Package NDC: | 0409-1171-01 |
Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1171-01) > 5 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 0409-1171-01 |
Proprietary Name | Diltiazem Hydrochloride |
Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1171-01) > 5 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 0409-1171 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Diltiazem Hydrochloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20120410 |
Marketing Category Name | ANDA |
Labeler Name | Hospira, Inc. |
Substance Name | DILTIAZEM HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |