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Claritin-D
Claritin-D - 11523-7162-3 - (Loratadine and pseudoephedrine sulfate)
Drug Information of Claritin-D
| Product NDC: | 11523-7162 |
| Proprietary Name: | Claritin-D |
| Non Proprietary Name: | Loratadine and pseudoephedrine sulfate |
| Active Ingredient(s): | 5; 120 mg/1; mg/1 & nbsp; Loratadine and pseudoephedrine sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Claritin-D
| Product NDC: | 11523-7162 |
| Labeler Name: | MSD Consumer Care, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA019670 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20091201 |
Package Information of Claritin-D
| Package NDC: | 11523-7162-3 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (11523-7162-3) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Claritin-D
| NDC Code | 11523-7162-3 |
| Proprietary Name | Claritin-D |
| Package Description | 3 BLISTER PACK in 1 CARTON (11523-7162-3) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 11523-7162 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loratadine and pseudoephedrine sulfate |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20091201 |
| Marketing Category Name | NDA |
| Labeler Name | MSD Consumer Care, Inc. |
| Substance Name | LORATADINE; PSEUDOEPHEDRINE SULFATE |
| Strength Number | 5; 120 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
