| NDC Code | 68462-353-01 |
|---|
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (68462-353-01) |
|---|
| Product NDC | 68462-353 |
|---|
| 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 | 20150201 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040812 |
|---|
| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
|---|
| Substance Name | HYDROXYZINE HYDROCHLORIDE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |
|---|