| NDC Code | 68788-6892-9 |
|---|
| Package Description | 90 TABLET in 1 BOTTLE (68788-6892-9) |
|---|
| Product NDC | 68788-6892 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Levocetirizine Dihydrochloride |
|---|
| Non-Proprietary Name | Levocetirizine Dihydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20170213 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203027 |
|---|
| Manufacturer | Preferred Pharmaceuticals Inc. |
|---|
| Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
|---|