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Hydroxyzine
Hydroxyzine - 52584-007-25 - (Hydroxyzine)
Drug Information of Hydroxyzine
| Product NDC: | 52584-007 |
| Proprietary Name: | Hydroxyzine |
| Non Proprietary Name: | Hydroxyzine |
| Active Ingredient(s): | 50 mg/mL & nbsp; Hydroxyzine |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydroxyzine
| Product NDC: | 52584-007 |
| Labeler Name: | General Injectables & Vaccines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087408 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100301 |
Package Information of Hydroxyzine
| Package NDC: | 52584-007-25 |
| Package Description: | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-007-25) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Hydroxyzine
| NDC Code | 52584-007-25 |
| Proprietary Name | Hydroxyzine |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-007-25) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 52584-007 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydroxyzine |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20100301 |
| Marketing Category Name | ANDA |
| Labeler Name | General Injectables & Vaccines, Inc |
| Substance Name | HYDROXYZINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |
