Product NDC: | 68788-9776 |
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) |
Product NDC: | 68788-9776 |
Labeler Name: | Preferred Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040010 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120727 |
Package NDC: | 68788-9776-4 |
Package Description: | 473 mL in 1 BOTTLE, PLASTIC (68788-9776-4) |
NDC Code | 68788-9776-4 |
Proprietary Name | HydrOXYzine Hydrochloride |
Package Description | 473 mL in 1 BOTTLE, PLASTIC (68788-9776-4) |
Product NDC | 68788-9776 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | HydrOXYzine Hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20120727 |
Marketing Category Name | ANDA |
Labeler Name | Preferred Pharmaceuticals, Inc. |
Substance Name | HYDROXYZINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |