| NDC Code | 60687-686-01 |
|---|
| Package Description | 100 BLISTER PACK in 1 CARTON (60687-686-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-686-11) |
|---|
| Product NDC | 60687-686 |
|---|
| 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 | 20221006 |
|---|
| End Marketing Date | 20241130 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA088619 |
|---|
| Manufacturer | American Health Packaging |
|---|
| Substance Name | HYDROXYZINE DIHYDROCHLORIDE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Antihistamine [EPC], Histamine Receptor Antagonists [MoA] |
|---|