| NDC Code | 37808-204-69 |
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| Package Description | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (37808-204-69) |
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| Product NDC | 37808-204 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Pseudoephedrine Hydrochloride |
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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 | 20060428 |
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| End Marketing Date | 20191031 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077442 |
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| Manufacturer | HEB |
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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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