| 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 |