| NDC Code | 51672-4161-5 |
|---|
| Package Description | 1 BOTTLE in 1 CARTON (51672-4161-5) / 177 mL in 1 BOTTLE |
|---|
| Product NDC | 51672-4161 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Levocetirizine Dihydrochloride |
|---|
| Non-Proprietary Name | Levocetirizine Dihydrochloride |
|---|
| Dosage Form | SOLUTION |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20130726 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202673 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
|---|
| Strength | .5 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
|---|