| NDC Code | 49999-771-90 |
|---|
| Package Description | 90 TABLET in 1 BOTTLE (49999-771-90) |
|---|
| Product NDC | 49999-771 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Fexofenadine Hydrochloride |
|---|
| Non-Proprietary Name | Fexofenadine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20091209 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076502 |
|---|
| Manufacturer | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
|---|
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
|---|
| Strength | 60 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
|---|