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Allergy Relief Non Drowsy
Allergy Relief Non Drowsy - 52904-430-01 - (Loratadine)
Drug Information of Allergy Relief Non Drowsy
| Product NDC: | 52904-430 |
| Proprietary Name: | Allergy Relief Non Drowsy |
| Non Proprietary Name: | Loratadine |
| Active Ingredient(s): | 10 mg/1 & nbsp; Loratadine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Allergy Relief Non Drowsy
| Product NDC: | 52904-430 |
| Labeler Name: | Select Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077153 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121015 |
Package Information of Allergy Relief Non Drowsy
| Package NDC: | 52904-430-01 |
| Package Description: | 1 TABLET in 1 PACKET (52904-430-01) |
NDC Information of Allergy Relief Non Drowsy
| NDC Code | 52904-430-01 |
| Proprietary Name | Allergy Relief Non Drowsy |
| Package Description | 1 TABLET in 1 PACKET (52904-430-01) |
| Product NDC | 52904-430 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loratadine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121015 |
| Marketing Category Name | ANDA |
| Labeler Name | Select Corporation |
| Substance Name | LORATADINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
