| NDC Code | 54868-5468-0 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (54868-5468-0) |
|---|
| Product NDC | 54868-5468 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Fexofenadine Hydrochloride |
|---|
| Non-Proprietary Name | Fexofenadine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20051109 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA020872 |
|---|
| Manufacturer | Physicians Total Care, Inc. |
|---|
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
|---|
| Strength | 30 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
|---|