Product NDC: | 11523-7200 |
Proprietary Name: | Claritin |
Non Proprietary Name: | Loratadine |
Active Ingredient(s): | 10 mg/1 & nbsp; Loratadine |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11523-7200 |
Labeler Name: | MSD Consumer Care, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA021952 |
Marketing Category: | NDA |
Start Marketing Date: | 20080616 |
Package NDC: | 11523-7200-3 |
Package Description: | 4 BLISTER PACK in 1 CARTON (11523-7200-3) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Code | 11523-7200-3 |
Proprietary Name | Claritin |
Package Description | 4 BLISTER PACK in 1 CARTON (11523-7200-3) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
Product NDC | 11523-7200 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Loratadine |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20080616 |
Marketing Category Name | NDA |
Labeler Name | MSD Consumer Care, Inc. |
Substance Name | LORATADINE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes |