| NDC Code | 63672-0051-0 |
|---|
| Package Description | 87000 TABLET, FILM COATED in 1 DRUM (63672-0051-0) |
|---|
| Product NDC | 63672-0051 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Levocetirizine Dihydrochloride |
|---|
| Non-Proprietary Name | Levocetirizine Dihydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20101126 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090229 |
|---|
| Manufacturer | Synthon Pharmaceuticals, Inc. |
|---|
| Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
|---|