| NDC Code | 68999-002-24 |
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| Package Description | 2 TRAY in 1 BOX (68999-002-24) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (68999-002-51) |
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| Product NDC | 68999-002 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Lactulose |
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| Non-Proprietary Name | Lactulose |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20181123 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA209517 |
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| Manufacturer | Chartwell Governmental & Specialty RX, LLC. |
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| Substance Name | LACTULOSE |
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| Strength | 10 |
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| Strength Unit | g/15mL |
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| Pharmacy Classes | Acidifying Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
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