Source: FDA, National Drug Code (US) Revision Year: 2020
Pretomanid is an oral nitroimidazooxazine antimycobacterial drug.
Pretomanid is a white to off-white to yellow-colored powder. The chemical name for pretomanid is (6S)-2-Nitro-6-{[4-(trifluoromethoxy)phenyl]methoxy}-6,7-dihydro-5Himidazo[2,1b][1,3]oxazine. The molecular formula for pretomanid is C14H12F3N3O5, and the molecular weight is 359.26. The structural formula of pretomanid is as follows:
Each Pretomanid Tablet contains 200 mg of pretomanid. The inactive ingredients are colloidal silicon dioxide, lactose monohydrate, magnesium stearate, microcrystalline cellulose, povidone, sodium lauryl sulfate, and sodium starch glycolate.
| Dosage Forms and Strengths |
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Pretomanid Tablets, 200 mg, are white to off-white oval tablets debossed with M on one side and P200 on the other side. |
| How Supplied | ||||||||
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Pretomanid Tablet 200 mg is packaged in either white, round, high-density polyethylene bottles with polypropylene child-resistant closure or child-resistant blister packages comprised of a polyvinylchloride film with foil and paper backing. Pretomanid Tablet 200 mg is a white to off-white, oval-shaped tablet debossed with M on one side and P200 on the other side.
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| Drug | Countries | |
|---|---|---|
| PRETOMANID | United States |
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