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allergy and congestion relief
allergy and congestion relief - 42507-724-22 - (Pseudoephedrine sulfate, Loratadine)
Drug Information of allergy and congestion relief
| Product NDC: | 42507-724 |
| Proprietary Name: | allergy and congestion relief |
| Non Proprietary Name: | Pseudoephedrine sulfate, Loratadine |
| Active Ingredient(s): | 10; 240 mg/1; mg/1 & nbsp; Pseudoephedrine sulfate, Loratadine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of allergy and congestion relief
| Product NDC: | 42507-724 |
| Labeler Name: | HyVee Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075989 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101026 |
Package Information of allergy and congestion relief
| Package NDC: | 42507-724-22 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (42507-724-22) > 5 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of allergy and congestion relief
| NDC Code | 42507-724-22 |
| Proprietary Name | allergy and congestion relief |
| Package Description | 3 BLISTER PACK in 1 CARTON (42507-724-22) > 5 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 42507-724 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pseudoephedrine sulfate, Loratadine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20101026 |
| Marketing Category Name | ANDA |
| Labeler Name | HyVee Inc |
| Substance Name | LORATADINE; PSEUDOEPHEDRINE SULFATE |
| Strength Number | 10; 240 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
