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Hydroxyzine Hydrochloride
Hydroxyzine Hydrochloride - 0517-5602-25 - (Hydroxyzine Hydrochloride)
Drug Information of Hydroxyzine Hydrochloride
| Product NDC: | 0517-5602 |
| Proprietary Name: | Hydroxyzine Hydrochloride |
| Non Proprietary Name: | Hydroxyzine Hydrochloride |
| Active Ingredient(s): | 50 mg/mL & nbsp; Hydroxyzine Hydrochloride |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydroxyzine Hydrochloride
| Product NDC: | 0517-5602 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087408 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19900930 |
Package Information of Hydroxyzine Hydrochloride
| Package NDC: | 0517-5602-25 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-5602-25) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Hydroxyzine Hydrochloride
| NDC Code | 0517-5602-25 |
| Proprietary Name | Hydroxyzine Hydrochloride |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-5602-25) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0517-5602 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydroxyzine Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 19900930 |
| Marketing Category Name | ANDA |
| Labeler Name | American Regent, Inc. |
| Substance Name | HYDROXYZINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |
