| NDC Code | 53808-0632-1 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0632-1) |
|---|
| Product NDC | 53808-0632 |
|---|
| 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 | 20130101 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040812 |
|---|
| Manufacturer | State of Florida DOH Central Pharmacy |
|---|
| Substance Name | HYDROXYZINE HYDROCHLORIDE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |
|---|