| NDC Code | 37808-724-69 |
|---|
| Package Description | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (37808-724-69) |
|---|
| Product NDC | 37808-724 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Loratadine And Pseudoephedrine Sulfate |
|---|
| Non-Proprietary Name | Loratadine And Pseudoephedrine Sulfate |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180201 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076557 |
|---|
| Manufacturer | HEB |
|---|
| Substance Name | LORATADINE; PSEUDOEPHEDRINE SULFATE |
|---|
| Strength | 10; 240 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC] |
|---|