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Hydralazine Hydrochloride
Hydralazine Hydrochloride - 63323-614-55 - (HYDRALAZINE HYDROCHLORIDE)
Drug Information of Hydralazine Hydrochloride
| Product NDC: | 63323-614 |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydralazine Hydrochloride
| Product NDC: | 63323-614 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040388 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010905 |
Package Information of Hydralazine Hydrochloride
| Package NDC: | 63323-614-55 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-614-55) > 1 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Hydralazine Hydrochloride
| NDC Code | 63323-614-55 |
| Proprietary Name | Hydralazine Hydrochloride |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-614-55) > 1 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 63323-614 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDRALAZINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20010905 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | HYDRALAZINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC] |
