NDC Code | 70934-891-15 |
Package Description | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-891-15) |
Product NDC | 70934-891 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Hydroxyzine Hydrochloride |
Non-Proprietary Name | Hydroxyzine Hydrochloride |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20210914 |
End Marketing Date | 20230331 |
Marketing Category Name | ANDA |
Application Number | ANDA088617 |
Manufacturer | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
Substance Name | HYDROXYZINE DIHYDROCHLORIDE |
Strength | 10 |
Strength Unit | mg/1 |
Pharmacy Classes | Antihistamine [EPC], Histamine Receptor Antagonists [MoA] |