| NDC Code | 68084-253-01 |
|---|
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-253-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-253-11) |
|---|
| Product NDC | 68084-253 |
|---|
| 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 | 20090114 |
|---|
| End Marketing Date | 20220630 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040786 |
|---|
| Manufacturer | American Health Packaging |
|---|
| Substance Name | HYDROXYZINE DIHYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Antihistamine [EPC], Histamine Receptor Antagonists [MoA] |
|---|