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allergy relief d
allergy relief d - 56062-165-22 - (Loratadine, Pseudoephedrine Sulfate)
Drug Information of allergy relief d
| Product NDC: | 56062-165 |
| Proprietary Name: | allergy relief d |
| Non Proprietary Name: | Loratadine, Pseudoephedrine Sulfate |
| Active Ingredient(s): | 10; 240 mg/1; mg/1 & nbsp; Loratadine, Pseudoephedrine Sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of allergy relief d
| Product NDC: | 56062-165 |
| Labeler Name: | Publix Super Markets Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075706 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030625 |
Package Information of allergy relief d
| Package NDC: | 56062-165-22 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (56062-165-22) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of allergy relief d
| NDC Code | 56062-165-22 |
| Proprietary Name | allergy relief d |
| Package Description | 3 BLISTER PACK in 1 CARTON (56062-165-22) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 56062-165 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loratadine, Pseudoephedrine Sulfate |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20030625 |
| Marketing Category Name | ANDA |
| Labeler Name | Publix Super Markets Inc |
| Substance Name | LORATADINE; PSEUDOEPHEDRINE SULFATE |
| Strength Number | 10; 240 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
