| NDC Code | 55111-784-18 |
|---|
| Package Description | 1 BOTTLE in 1 CARTON (55111-784-18) / 180 TABLET in 1 BOTTLE |
|---|
| Product NDC | 55111-784 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Fexofenadine Hydrochloride |
|---|
| Non-Proprietary Name | Fexofenadine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20110103 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076502 |
|---|
| Manufacturer | Dr. Reddy's Laboratories Limited |
|---|
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
|---|
| Strength | 180 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
|---|