| NDC Code | 57664-112-88 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE (57664-112-88) |
|---|
| Product NDC | 57664-112 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Hydroxyzine Hydrochloride |
|---|
| Non-Proprietary Name | Hydroxyzine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20090331 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040899 |
|---|
| Manufacturer | Caraco Pharmaceutical Laboratories, Ltd. |
|---|
| Substance Name | HYDROXYZINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |
|---|