Product NDC: | 0904-5806 |
Proprietary Name: | Loratadine ODT |
Non Proprietary Name: | Loratadine |
Active Ingredient(s): | 10 mg/1 & nbsp; Loratadine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0904-5806 |
Labeler Name: | Major Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA077153 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070831 |
Package NDC: | 0904-5806-15 |
Package Description: | 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0904-5806-15) |
NDC Code | 0904-5806-15 |
Proprietary Name | Loratadine ODT |
Package Description | 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0904-5806-15) |
Product NDC | 0904-5806 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Loratadine |
Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
Route Name | ORAL |
Start Marketing Date | 20070831 |
Marketing Category Name | ANDA |
Labeler Name | Major Pharmaceuticals |
Substance Name | LORATADINE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes |