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HydrOXYzine Hydrochloride
HydrOXYzine Hydrochloride - 50383-796-16 - (HydrOXYzine Hydrochloride)
Drug Information of HydrOXYzine Hydrochloride
| Product NDC: | 50383-796 |
| Proprietary Name: | HydrOXYzine Hydrochloride |
| Non Proprietary Name: | HydrOXYzine Hydrochloride |
| Active Ingredient(s): | 10 mg/5mL & nbsp; HydrOXYzine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HydrOXYzine Hydrochloride
| Product NDC: | 50383-796 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040010 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19941028 |
Package Information of HydrOXYzine Hydrochloride
| Package NDC: | 50383-796-16 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (50383-796-16) |
NDC Information of HydrOXYzine Hydrochloride
| NDC Code | 50383-796-16 |
| Proprietary Name | HydrOXYzine Hydrochloride |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (50383-796-16) |
| Product NDC | 50383-796 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HydrOXYzine Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19941028 |
| Marketing Category Name | ANDA |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | HYDROXYZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |
