Home
>
National Drug Code (NDC)
>
Allergy Relief
Allergy Relief - 51660-527-31 - (Loratadine)
Drug Information of Allergy Relief
| Product NDC: | 51660-527 |
| Proprietary Name: | Allergy Relief |
| Non Proprietary Name: | Loratadine |
| Active Ingredient(s): | 10 mg/1 & nbsp; Loratadine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Allergy Relief
| Product NDC: | 51660-527 |
| Labeler Name: | Ohm Laboratories Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077153 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070831 |
Package Information of Allergy Relief
| Package NDC: | 51660-527-31 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (51660-527-31) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (51660-527-69) |
NDC Information of Allergy Relief
| NDC Code | 51660-527-31 |
| Proprietary Name | Allergy Relief |
| Package Description | 3 BLISTER PACK in 1 CARTON (51660-527-31) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (51660-527-69) |
| Product NDC | 51660-527 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loratadine |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20070831 |
| Marketing Category Name | ANDA |
| Labeler Name | Ohm Laboratories Inc. |
| Substance Name | LORATADINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
