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KU 210 (Montelukast sodium 10 mg (base))

This pill with imprint "KU 210" is White, Round and has been identified as Montelukast sodium 10 mg (base). It is manufactured by Kremers Urban Pharmaceuticals Inc..

Montelukast is used in the treatment of allergic rhinitis; asthma, maintenance; bronchospasm prophylaxis; copd; asthma and belongs to the drug class leukotriene modifiers. There is no proven risk in humans during pregnancy. Montelukast 10 mg (base) is not a controlled substance under the Controlled Substance Act (CSA).

Montelukast sodium 10 mg (base) KU 210
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Montelukast sodium
Imprint:
KU 210
Strength:
10 mg (base)
Color:
White
Shape:
Round
Availability:
Prescription only
Drug Class:
Leukotriene modifiers
Pregnancy Category:
B - No proven risk in humans
CSA Schedule:
Not a controlled drug
Manufacturer:
Kremers Urban Pharmaceuticals Inc.
National Drug Code (NDC):
62175-0210
Inactive Ingredients:
silicon dioxide
croscarmellose sodium
hydroxypropyl cellulose (type h)
mannitol
microcrystalline cellulose
polyethylene glycol
polyvinyl alcohol
sodium stearyl fumarate
magnesium silicate
titanium dioxide

Note: Inactive ingredients may vary.

Imprint Code FAQ's

Other Manufacturers / Repackagers:
NDC CodeManufacturer / Repackager
42291-0621 AvKare, Inc.

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