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allergy relief medication
allergy relief medication - 11673-315-30 - (loratadine)
Drug Information of allergy relief medication
| Product NDC: | 11673-315 |
| Proprietary Name: | allergy relief medication |
| 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 medication
| Product NDC: | 11673-315 |
| Labeler Name: | Target Brands, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075209 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100131 |
Package Information of allergy relief medication
| Package NDC: | 11673-315-30 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (11673-315-30) > 10 TABLET in 1 BLISTER PACK |
NDC Information of allergy relief medication
| NDC Code | 11673-315-30 |
| Proprietary Name | allergy relief medication |
| Package Description | 3 BLISTER PACK in 1 CARTON (11673-315-30) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 11673-315 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | loratadine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100131 |
| Marketing Category Name | ANDA |
| Labeler Name | Target Brands, Inc. |
| Substance Name | LORATADINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
