Product NDC: | 47682-203 |
Proprietary Name: | MEDIQUE Loradamed |
Non Proprietary Name: | Loratadine |
Active Ingredient(s): | 10 mg/1 & nbsp; Loratadine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 47682-203 |
Labeler Name: | Unifirst First Aid Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA076134 |
Marketing Category: | ANDA |
Start Marketing Date: | 20081230 |
Package NDC: | 47682-203-50 |
Package Description: | 50 PACKET in 1 BOX, UNIT-DOSE (47682-203-50) > 1 TABLET, FILM COATED in 1 PACKET (47682-203-46) |
NDC Code | 47682-203-50 |
Proprietary Name | MEDIQUE Loradamed |
Package Description | 50 PACKET in 1 BOX, UNIT-DOSE (47682-203-50) > 1 TABLET, FILM COATED in 1 PACKET (47682-203-46) |
Product NDC | 47682-203 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Loratadine |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20081230 |
Marketing Category Name | ANDA |
Labeler Name | Unifirst First Aid Corporation |
Substance Name | LORATADINE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes |