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Sunmark Loratadine
Sunmark Loratadine - 49348-818-13 - (Loratadine)
Drug Information of Sunmark Loratadine
| Product NDC: | 49348-818 |
| Proprietary Name: | Sunmark 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 Sunmark Loratadine
| Product NDC: | 49348-818 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076301 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070621 |
Package Information of Sunmark Loratadine
| Package NDC: | 49348-818-13 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-818-13) > 90 TABLET in 1 BOTTLE |
NDC Information of Sunmark Loratadine
| NDC Code | 49348-818-13 |
| Proprietary Name | Sunmark Loratadine |
| Package Description | 1 BOTTLE in 1 CARTON (49348-818-13) > 90 TABLET in 1 BOTTLE |
| Product NDC | 49348-818 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loratadine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070621 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | LORATADINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
