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allergy relief
allergy relief - 0067-6066-05 - (loratadine)
Drug Information of allergy relief
| Product NDC: | 0067-6066 |
| Proprietary Name: | allergy relief |
| 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
| Product NDC: | 0067-6066 |
| Labeler Name: | Novartis Consumer Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA075209 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100104 |
Package Information of allergy relief
| Package NDC: | 0067-6066-05 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (0067-6066-05) > 5 TABLET in 1 BLISTER PACK |
NDC Information of allergy relief
| NDC Code | 0067-6066-05 |
| Proprietary Name | allergy relief |
| Package Description | 1 BLISTER PACK in 1 CARTON (0067-6066-05) > 5 TABLET in 1 BLISTER PACK |
| Product NDC | 0067-6066 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | loratadine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100104 |
| Marketing Category Name | NDA |
| Labeler Name | Novartis Consumer Health, Inc. |
| Substance Name | LORATADINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
