NDC Code | 0378-2586-10 |
Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-2586-10) |
Product NDC | 0378-2586 |
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 | 20100723 |
End Marketing Date | 20190930 |
Marketing Category Name | ANDA |
Application Number | ANDA091176 |
Manufacturer | Mylan Pharmaceuticals Inc. |
Substance Name | HYDROXYZINE HYDROCHLORIDE |
Strength | 10 |
Strength Unit | mg/1 |
Pharmacy Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |