Product NDC: | 0363-0165 |
Proprietary Name: | Wal itin D |
Non Proprietary Name: | Loratadine, Pseudoephedrine Sulfate |
Active Ingredient(s): | 10; 240 mg/1; mg/1 & nbsp; Loratadine, Pseudoephedrine Sulfate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0363-0165 |
Labeler Name: | Walgreen Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA075706 |
Marketing Category: | ANDA |
Start Marketing Date: | 20030604 |
Package NDC: | 0363-0165-22 |
Package Description: | 3 BLISTER PACK in 1 CARTON (0363-0165-22) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Code | 0363-0165-22 |
Proprietary Name | Wal itin D |
Package Description | 3 BLISTER PACK in 1 CARTON (0363-0165-22) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 0363-0165 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Loratadine, Pseudoephedrine Sulfate |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20030604 |
Marketing Category Name | ANDA |
Labeler Name | Walgreen Company |
Substance Name | LORATADINE; PSEUDOEPHEDRINE SULFATE |
Strength Number | 10; 240 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |