Source: FDA, National Drug Code (US) Revision Year: 2020
MYAMBUTOL ethambutol hydrochloride is an oral chemotherapeutic agent which is specifically effective against actively growing microorganisms of the genus Mycobacterium, including M. tuberculosis.
The structural formula is:
MYAMBUTOL 100 and 400 mg tablets contain the following inactive ingredients: Gelatin, Hydroxypropyl Methylcellulose, Magnesium Stearate, Sodium Lauryl Sulfate, Sorbitol, Stearic Acid, Sucrose, Titanium Dioxide and other ingredients.
| How Supplied |
|---|
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MYAMBUTOL (Ethambutol Hydrochloride) Tablets USP 100 mg – round, convex, white, film coated tablets engraved with M6 on one side are supplied as follows: NDC 68850-010-01 – Bottle of 100 400 mg – round, convex, white, scored, film coated tablets engraved with M to the left and 7 to the right of the score on one side are NDC 68850-012-01 – Bottle of 100 Manufactured by Patheon Inc., Ontario, Canada. |
| Drug | Countries | |
|---|---|---|
| MYAMBUTOL | Austria, Spain, France, Malta, Netherlands, United States |
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