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Loratadine
Loratadine - 50436-3501-2 - (Loratadine)
Drug Information of Loratadine
| Product NDC: | 50436-3501 |
| Proprietary Name: | Loratadine |
| 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 Loratadine
| Product NDC: | 50436-3501 |
| Labeler Name: | Unit Dose Services |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076301 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081015 |
Package Information of Loratadine
| Package NDC: | 50436-3501-2 |
| Package Description: | 30 TABLET in 1 BOTTLE (50436-3501-2) |
NDC Information of Loratadine
| NDC Code | 50436-3501-2 |
| Proprietary Name | Loratadine |
| Package Description | 30 TABLET in 1 BOTTLE (50436-3501-2) |
| Product NDC | 50436-3501 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loratadine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20081015 |
| Marketing Category Name | ANDA |
| Labeler Name | Unit Dose Services |
| Substance Name | LORATADINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
