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Diltiazem Hydrochloride
Diltiazem Hydrochloride - 10019-510-01 - (Diltiazem Hydrochloride)
Drug Information of Diltiazem Hydrochloride
| Product NDC: | 10019-510 |
| 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) |
Labeler Information of Diltiazem Hydrochloride
| Product NDC: | 10019-510 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078538 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100713 |
Package Information of Diltiazem Hydrochloride
| Package NDC: | 10019-510-01 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 PACKAGE (10019-510-01) > 5 mL in 1 VIAL, SINGLE-DOSE (10019-510-79) |
NDC Information of Diltiazem Hydrochloride
| NDC Code | 10019-510-01 |
| Proprietary Name | Diltiazem Hydrochloride |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 PACKAGE (10019-510-01) > 5 mL in 1 VIAL, SINGLE-DOSE (10019-510-79) |
| Product NDC | 10019-510 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diltiazem Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100713 |
| Marketing Category Name | ANDA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | DILTIAZEM HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
