NDC Code | 70934-716-60 |
Package Description | 60 TABLET in 1 BOTTLE, PLASTIC (70934-716-60) |
Product NDC | 70934-716 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Hydroxyzine Hydrochloride |
Non-Proprietary Name | Hydroxyzine Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20200519 |
Marketing Category Name | ANDA |
Application Number | ANDA204279 |
Manufacturer | Denton Pharma, Inc. dba Northwind Pharmaceuticals |
Substance Name | HYDROXYZINE DIHYDROCHLORIDE |
Strength | 25 |
Strength Unit | mg/1 |
Pharmacy Classes | Antihistamine [EPC], Histamine Receptor Antagonists [MoA] |