| NDC Code | 37808-427-69 |
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| Package Description | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (37808-427-69) |
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| Product NDC | 37808-427 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Loratadine And Pseudoephedrine Sulfate |
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| Non-Proprietary Name | Loratadine And Pseudoephedrine Sulfate |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20180201 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076557 |
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| Manufacturer | HEB |
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| Substance Name | LORATADINE; PSEUDOEPHEDRINE SULFATE |
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| Strength | 10; 240 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC] |
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