| NDC Code | 70677-0036-1 |
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| Package Description | 20 BLISTER PACK in 1 CARTON (70677-0036-1) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
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| Product NDC | 70677-0036 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Sunmark 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 | 20180604 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076050 |
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| Manufacturer | Strategic Sourcing Services LLC |
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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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