| NDC Code | 53002-3901-3 |
|---|
| Package Description | 30 TABLET in 1 BOTTLE (53002-3901-3) |
|---|
| Product NDC | 53002-3901 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Hydroxyzine Hydrochloride |
|---|
| Non-Proprietary Name | Hydroxyzine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20140820 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA204279 |
|---|
| Manufacturer | RPK Pharmaceuticals, Inc. |
|---|
| Substance Name | HYDROXYZINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Antihistamine [EPC], Histamine Receptor Antagonists [MoA] |
|---|