NDC Code | 41250-724-69 |
Package Description | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (41250-724-69) |
Product NDC | 41250-724 |
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 | 20041117 |
Marketing Category Name | ANDA |
Application Number | ANDA076557 |
Manufacturer | Meijer Distribution, Inc. |
Substance Name | LORATADINE; PSEUDOEPHEDRINE SULFATE |
Strength | 10; 240 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC] |