Product NDC: | 0603-3968 |
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, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0603-3968 |
Labeler Name: | Qualitest Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040574 |
Marketing Category: | ANDA |
Start Marketing Date: | 20050527 |
Package NDC: | 0603-3968-32 |
Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0603-3968-32) |
NDC Code | 0603-3968-32 |
Proprietary Name | Hydroxyzine Hydrochloride |
Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0603-3968-32) |
Product NDC | 0603-3968 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | hydroxyzine hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20050527 |
Marketing Category Name | ANDA |
Labeler Name | Qualitest Pharmaceuticals |
Substance Name | HYDROXYZINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |