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Hydralazine Hydrochloride
Hydralazine Hydrochloride - 0517-0901-25 - (Hydralazine Hydrochloride)
Drug Information of Hydralazine Hydrochloride
| Product NDC: | 0517-0901 |
| Proprietary Name: | Hydralazine Hydrochloride |
| Non Proprietary Name: | Hydralazine Hydrochloride |
| Active Ingredient(s): | 20 mg/mL & nbsp; Hydralazine Hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydralazine Hydrochloride
| Product NDC: | 0517-0901 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040136 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970630 |
Package Information of Hydralazine Hydrochloride
| Package NDC: | 0517-0901-25 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-0901-25) > 1 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Hydralazine Hydrochloride
| NDC Code | 0517-0901-25 |
| Proprietary Name | Hydralazine Hydrochloride |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-0901-25) > 1 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0517-0901 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydralazine Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19970630 |
| Marketing Category Name | ANDA |
| Labeler Name | American Regent, Inc. |
| Substance Name | HYDRALAZINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC] |
