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Diltiazem Hydrochloride
Diltiazem Hydrochloride - 0409-4350-03 - (DILTIAZEM HYDROCHLORIDE)
Drug Information of Diltiazem Hydrochloride
| Product NDC: | 0409-4350 |
| Proprietary Name: | Diltiazem Hydrochloride |
| Non Proprietary Name: | DILTIAZEM HYDROCHLORIDE |
| Active Ingredient(s): | 100 mg/1 & nbsp; DILTIAZEM HYDROCHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diltiazem Hydrochloride
| Product NDC: | 0409-4350 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075853 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111020 |
Package Information of Diltiazem Hydrochloride
| Package NDC: | 0409-4350-03 |
| Package Description: | 10 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-4350-03) > 1 POWDER, FOR SOLUTION in 1 VIAL, PATENT DELIVERY SYSTEM |
NDC Information of Diltiazem Hydrochloride
| NDC Code | 0409-4350-03 |
| Proprietary Name | Diltiazem Hydrochloride |
| Package Description | 10 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-4350-03) > 1 POWDER, FOR SOLUTION in 1 VIAL, PATENT DELIVERY SYSTEM |
| Product NDC | 0409-4350 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DILTIAZEM HYDROCHLORIDE |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20111020 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | DILTIAZEM HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
