| NDC Code | 50580-670-30 |
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| Package Description | 3 CARTON in 1 PACKAGE (50580-670-30) > 1 BLISTER PACK in 1 CARTON (50580-670-10) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
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| Product NDC | 50580-670 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Sudafed 12 Hour |
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| Non-Proprietary Name | Pseudoephedrine Hydrochloride |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20080601 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA073585 |
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| Manufacturer | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
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| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
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| Strength | 120 |
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| Strength Unit | mg/1 |
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