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HydrOXYzine hydrochloride
HydrOXYzine hydrochloride - 57664-113-18 - (HydrOXYzine hydrochloride)
Drug Information of HydrOXYzine hydrochloride
| Product NDC: | 57664-113 |
| Proprietary Name: | HydrOXYzine hydrochloride |
| Non Proprietary Name: | HydrOXYzine hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; HydrOXYzine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HydrOXYzine hydrochloride
| Product NDC: | 57664-113 |
| Labeler Name: | Caraco Pharmaceutical Laboratories, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040899 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090331 |
Package Information of HydrOXYzine hydrochloride
| Package NDC: | 57664-113-18 |
| Package Description: | 1000 TABLET in 1 BOTTLE (57664-113-18) |
NDC Information of HydrOXYzine hydrochloride
| NDC Code | 57664-113-18 |
| Proprietary Name | HydrOXYzine hydrochloride |
| Package Description | 1000 TABLET in 1 BOTTLE (57664-113-18) |
| Product NDC | 57664-113 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HydrOXYzine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090331 |
| Marketing Category Name | ANDA |
| Labeler Name | Caraco Pharmaceutical Laboratories, Ltd. |
| Substance Name | HYDROXYZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |
