Product NDC: | 54569-1640 |
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): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54569-1640 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA087294 |
Marketing Category: | ANDA |
Start Marketing Date: | 19950309 |
Package NDC: | 54569-1640-1 |
Package Description: | 120 mL in 1 BOTTLE, PLASTIC (54569-1640-1) |
NDC Code | 54569-1640-1 |
Proprietary Name | Hydroxyzine Hydrochloride |
Package Description | 120 mL in 1 BOTTLE, PLASTIC (54569-1640-1) |
Product NDC | 54569-1640 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hydroxyzine Hydrochloride |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 19950309 |
Marketing Category Name | ANDA |
Labeler Name | A-S Medication Solutions LLC |
Substance Name | HYDROXYZINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |