| NDC Code | 41415-994-36 |
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| Package Description | 2 BLISTER PACK in 1 CARTON (41415-994-36) > 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
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| Product NDC | 41415-994 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Guaifenesin And Pseudoephedrine Hydrochloride |
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| Non-Proprietary Name | Guaifenesin And Pseudoephedrine Hydrochloride |
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| Dosage Form | TABLET, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20220407 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212542 |
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| Manufacturer | PUBLIX SUPER MARKETS, INC |
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| Substance Name | GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
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| Strength | 600; 60 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic alpha-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-Adrenergic Agonist [EPC] |
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