Product NDC: | 68084-253 |
Proprietary Name: | HYDROXYZINE HYDROCHLORIDE |
Non Proprietary Name: | HYDROXYZINE HYDROCHLORIDE |
Active Ingredient(s): | 10 mg/1 & nbsp; HYDROXYZINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68084-253 |
Labeler Name: | American Health Packaging |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040786 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090113 |
Package NDC: | 68084-253-01 |
Package Description: | 10 BLISTER PACK in 1 CARTON (68084-253-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-253-11) |
NDC Code | 68084-253-01 |
Proprietary Name | HYDROXYZINE HYDROCHLORIDE |
Package Description | 10 BLISTER PACK in 1 CARTON (68084-253-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-253-11) |
Product NDC | 68084-253 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | HYDROXYZINE HYDROCHLORIDE |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20090113 |
Marketing Category Name | ANDA |
Labeler Name | American Health Packaging |
Substance Name | HYDROXYZINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |