| NDC Code | 43598-892-07 |
|---|
| Package Description | 1 BLISTER PACK in 1 CARTON (43598-892-07) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
|---|
| Product NDC | 43598-892 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Fexofenadine Hcl And Pseudoephedrine Hcl |
|---|
| Non-Proprietary Name | Fexofenadine Hcl And Pseudoephedrine Hcl |
|---|
| Dosage Form | TABLET, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20220517 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA079043 |
|---|
| Manufacturer | Dr.Reddy's Laboratories Inc |
|---|
| Substance Name | FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
|---|
| Strength | 180; 240 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Adrenergic alpha-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-Adrenergic Agonist [EPC] |
|---|