| NDC Code | 0093-5060-05 |
|---|
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (0093-5060-05) |
|---|
| Product NDC | 0093-5060 |
|---|
| 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 | 20130219 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA088617 |
|---|
| Manufacturer | Teva Pharmaceuticals USA, Inc. |
|---|
| Substance Name | HYDROXYZINE DIHYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Antihistamine [EPC], Histamine Receptor Antagonists [MoA] |
|---|