| NDC Code | 52389-155-02 |
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| Package Description | 2 BOTTLE, PLASTIC in 1 PACKAGE (52389-155-02) / 80 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
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| Product NDC | 52389-155 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Diurex |
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| Proprietary Name Suffix | Ultra |
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| Non-Proprietary Name | Caffeine |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20050901 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M027 |
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| Manufacturer | Kobayashi Healthcare International, Inc. |
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| Substance Name | CAFFEINE |
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| Strength | 100 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS] |
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