| NDC Code | 65193-125-48 |
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| Package Description | 48 TABLET in 1 BLISTER PACK (65193-125-48) |
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| Product NDC | 65193-125 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Red Label Ephedrine Plus |
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| Non-Proprietary Name | Ephedrine Hydrochloride, Guaifenesin |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20190402 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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| Manufacturer | Dickey Consumer Products DBA DMD |
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| Substance Name | EPHEDRINE HYDROCHLORIDE; GUAIFENESIN |
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| Strength | 12.5; 200 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Increased Norepinephrine Activity [PE], Norepinephrine Releasing Agent [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] |
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