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HYDROXYZINE HYDROCHLORIDE
HYDROXYZINE HYDROCHLORIDE - 68084-254-01 - (HYDROXYZINE HYDROCHLORIDE)
Drug Information of HYDROXYZINE HYDROCHLORIDE
| Product NDC: | 68084-254 |
| 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) |
Labeler Information of HYDROXYZINE HYDROCHLORIDE
| Product NDC: | 68084-254 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040787 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090113 |
Package Information of HYDROXYZINE HYDROCHLORIDE
| Package NDC: | 68084-254-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-254-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-254-11) |
NDC Information of HYDROXYZINE HYDROCHLORIDE
| NDC Code | 68084-254-01 |
| Proprietary Name | HYDROXYZINE HYDROCHLORIDE |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-254-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-254-11) |
| Product NDC | 68084-254 |
| 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 | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |
