NDC Code | 53217-225-30 |
Package Description | 30 TABLET in 1 BOTTLE (53217-225-30) |
Product NDC | 53217-225 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Hydroxyzine Hydrochloride |
Non-Proprietary Name | Hydroxyzine Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20120324 |
Marketing Category Name | ANDA |
Application Number | ANDA204279 |
Manufacturer | Aidarex Pharmaceuticals LLC |
Substance Name | HYDROXYZINE HYDROCHLORIDE |
Strength | 50 |
Strength Unit | mg/1 |
Pharmacy Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |