| NDC Code | 45802-122-60 |
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| Package Description | 20 BLISTER PACK in 1 CARTON (45802-122-60) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
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| Product NDC | 45802-122 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Loratadine D |
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| Non-Proprietary Name | Loratadine, 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 | 20180410 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076050 |
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| Manufacturer | Padagis Israel Pharmaceuticals Ltd |
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| Substance Name | LORATADINE; PSEUDOEPHEDRINE SULFATE |
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| Strength | 5; 120 |
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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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