| NDC Code | 41163-165-52 |
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| Package Description | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (41163-165-52) |
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| Product NDC | 41163-165 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Loratadine And Pseudoephedrine |
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| Non-Proprietary Name | Loratadine And Pseudoephedrine |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20041117 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076557 |
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| Manufacturer | SUPERVALU INC. |
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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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